Canonical Allele Identifier: PA2829314061
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1051083
ClinVar RCV Id: RCV001359074

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001387599.1:p.Asp223Asn
CA2053646
NM_001400670.1:c.667G>A