Canonical Allele Identifier: PA658800616
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 523313
ClinVar RCV Id: RCV000626571 RCV001051234 RCV001815421
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000034.1:p.Leu179Arg
CA377509124
NM_000043.6:c.536T>G