Allele Registry

Canonical Allele Identifier: PA126577

Gene: FAS HGNC NCBI

ClinVar RCV:

RCV000017966

ClinVar Variation:

16502

HGVS (amino-acid)	Matching Registered Transcripts
NP_690611.1:p.Arg121Trp	CA126574 NM_152872.4:c.361C>T