Canonical Allele Identifier: PA2826283714
Gene: CASP10 HGNC NCBI

Linked Data

ClinVar Variation Id: 7768

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193453.1:p.Met147Thr
CA210523
NM_001206524.2:c.440T>C