Allele Registry

Canonical Allele Identifier: PA091557

Gene: FAS HGNC NCBI

ClinVar RCV:

RCV000017966

ClinVar Variation:

16502

HGVS (amino-acid)	Matching Registered Transcripts
NP_000034.1:p.Arg121Trp	CA126574 NM_000043.6:c.361C>T