Canonical Allele Identifier: PA645397444
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 301530
ClinVar RCV Id: RCV000343056 RCV000444947
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000034.1:p.Ile184Val
CA5593154
NM_000043.6:c.550A>G