Canonical Allele Identifier: PA1139669892
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 863735
ClinVar RCV Id: RCV001070775
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000034.1:p.Gly253Val
CA377509733
NM_000043.6:c.758G>T