Canonical Allele Identifier: PA2830106475
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 7760
ClinVar RCV Id: RCV000008201

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_203520.1:p.Arg233Trp
CA119046
NM_033356.4:c.697C>T