Canonical Allele Identifier: PA2829310139
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 7760
ClinVar RCV Id: RCV000008201

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387571.1:p.Arg292Trp
CA119046
NM_001400642.1:c.874C>T