Allele Registry

Canonical Allele Identifier: PA126605

Gene: FAS HGNC NCBI

ClinVar RCV:

RCV000017977

ClinVar Variation:

16513

HGVS (amino-acid)	Matching Registered Transcripts
NP_000034.1:p.Gly247Ala	CA126602 NM_000043.6:c.740G>C