Canonical Allele Identifier: PA2829311822
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1721167
ClinVar RCV Id: RCV002294857

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387586.1:p.Arg233Gly
CA350293892
NM_001400657.1:c.697C>G