Canonical Allele Identifier: PA2830108855
Gene: CASP10 HGNC NCBI

Linked Data

ClinVar Variation Id: 333436
ClinVar RCV Id: RCV000334321

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116756.2:p.Gly439Val
CA10612331
NM_032974.5:c.1316G>T