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Human Genome Region ASPN

Assembly:
GRCh38.p14
Location:
chr9:92,165,272-92,647,523
Cytogenetic location:

No associated genome issues

Patches and alternate loci
Show in Viewer GenBank ID RefSeq ID Scaffold type Length Alignment mismatch Unique sequence
MU273365.1 Not yet assigned FIX Unavailable Unavailable Unavailable
           

ASPN -- chr9 (CM000671.2):92,165,272-92,647,523