Canonical Allele Identifier: PA2830106248
Gene: CASP8 HGNC NCBI

Linked Data

ClinVar Variation Id: 1051083
ClinVar RCV Id: RCV001359074

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_203519.1:p.Asp223Asn
CA2053646
NM_033355.3:c.667G>A