Canonical Allele Identifier: PA2829314476
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1051083
ClinVar RCV Id: RCV001359074

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387603.1:p.Asp18Asn
CA2053646
NM_001400674.1:c.52G>A