Canonical Allele Identifier: PA2826284118
Gene: CASP10 HGNC NCBI

Linked Data

ClinVar Variation Id: 897316

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193471.1:p.Lys262Glu
CA2053093
NM_001206542.2:c.784A>G