Canonical Allele Identifier: PA159639
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 134374
ClinVar RCV Id: RCV000121048 RCV000407819 RCV000766928 RCV003935155
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000034.1:p.Glu194Lys
CA159637
NM_000043.6:c.580G>A