Canonical Allele Identifier: PA2825026456
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2050141
ClinVar RCV Id: RCV002914366
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000034.1:p.Val227Ala
CA377509532
NM_000043.6:c.680T>C