Allele Registry

Canonical Allele Identifier: PA091561

Gene: FAS HGNC NCBI

ClinVar RCV:

RCV000017980

ClinVar Variation:

16516

HGVS (amino-acid)	Matching Registered Transcripts
NP_000034.1:p.Asp260Tyr	CA126607 NM_000043.6:c.778G>T