Canonical Allele Identifier: PA2826283880
Gene: CASP10 HGNC NCBI

Linked Data

ClinVar Variation Id: 643723

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193453.1:p.Ala374Thr
CA2053221
NM_001206524.2:c.1120G>A