Allele Registry

Canonical Allele Identifier: PA091572

Gene: FAS HGNC NCBI

ClinVar RCV:

RCV000017963

ClinVar Variation:

16499

HGVS (amino-acid)	Matching Registered Transcripts
NP_000034.1:p.Thr241Pro	CA126567 NM_000043.6:c.721A>C