Canonical Allele Identifier: PA2573159969
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 1368062
ClinVar RCV Id: RCV001874318
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000034.1:p.Val245Gly
CA211334978
NM_000043.6:c.734T>G