Canonical Allele Identifier: PA2829312041
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 533732
ClinVar RCV Id: RCV000640975

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387587.1:p.Ile283Val
CA2053716
NM_001400658.1:c.847A>G