Canonical Allele Identifier: PA2826284196
Gene: CASP10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1494185
ClinVar RCV Id: RCV001987054

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193471.1:p.Val409Ala
CA2053229
NM_001206542.2:c.1226T>C