Canonical Allele Identifier: PA2829313122
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1051083
ClinVar RCV Id: RCV001359074

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387593.1:p.Asp200Asn
CA2053646
NM_001400664.1:c.598G>A