Canonical Allele Identifier: PA2829314100
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1721167
ClinVar RCV Id: RCV002294857

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387600.1:p.Arg34Gly
CA350293892
NM_001400671.1:c.100C>G