Canonical Allele Identifier: PA2825026513
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2955291
ClinVar RCV Id: RCV003818466
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000034.1:p.Asp321Glu
CA377510206
NM_000043.6:c.963C>A
CA377510207
NM_000043.6:c.963C>G