Canonical Allele Identifier: PA2830106466
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1721167
ClinVar RCV Id: RCV002294857

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_203520.1:p.Arg218Gly
CA350293892
NM_033356.4:c.652C>G