Canonical Allele Identifier: PA2826284119
Gene: CASP10 HGNC NCBI

Linked Data

ClinVar Variation Id: 535757
ClinVar RCV Id: RCV001796759

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193471.1:p.Ala264Asp
CA350287126
NM_001206542.2:c.791C>A