Canonical Allele Identifier: PA095169
Gene: CASP10 HGNC NCBI

Linked Data

ClinVar Variation Id: 7768

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116756.2:p.Met147Thr
CA210523
NM_032974.5:c.440T>C