Canonical Allele Identifier: PA915955276
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 636699
ClinVar RCV Id: RCV000788605
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000034.1:p.Glu272Ala
CA377509874
NM_000043.6:c.815A>C