Canonical Allele Identifier: PA2829311450
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 7760
ClinVar RCV Id: RCV000008201

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387584.1:p.Arg248Trp
CA119046
NM_001400655.1:c.742C>T