Canonical Allele Identifier: PA2825026485
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 2764356
ClinVar RCV Id: RCV003517664
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000034.1:p.Lys274Glu
CA377509886
NM_000043.6:c.820A>G