Allele Registry

Canonical Allele Identifier: PA2827048350

Gene: FAS HGNC NCBI

ClinVar Variation Id: 523313

HGVS (amino-acid)	Matching Registered Transcripts
NP_001307548.1:p.Leu179Arg	CA377509124 NM_001320619.2:c.536T>G