Canonical Allele Identifier: PA2829317149
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 845577

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387680.1:p.Asp45Asn
CA2053660
NM_001400751.1:c.133G>A