Canonical Allele Identifier: PA2826284048
Gene: CASP10 HGNC NCBI

Linked Data

ClinVar Variation Id: 7768

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193471.1:p.Met147Thr
CA210523
NM_001206542.2:c.440T>C