Allele Registry

Canonical Allele Identifier: PA126609

Gene: FAS HGNC NCBI

ClinVar RCV:

RCV000017980

ClinVar Variation:

16516

HGVS (amino-acid)	Matching Registered Transcripts
NP_690610.1:p.Asp239Tyr	CA126607 NM_152871.4:c.715G>T