Canonical Allele Identifier: PA2829317141
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 642198
ClinVar RCV Id: RCV000795615

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387680.1:p.Gly20Glu
CA350293942
NM_001400751.1:c.59G>A