Canonical Allele Identifier: PA658800617
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 522316
ClinVar RCV Id: RCV000625369 RCV000658571
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000034.1:p.Lys193Arg
CA5593165
NM_000043.6:c.578A>G