Canonical Allele Identifier: PA159642
Gene: FAS HGNC NCBI

Linked Data

ClinVar Variation Id: 134375
ClinVar RCV Id: RCV000121049
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000034.1:p.Asn252Lys
CA159640
NM_000043.6:c.756T>G
CA377509726
NM_000043.6:c.756T>A