Canonical Allele Identifier: PA2830108872
Gene: CASP10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1951627

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116756.2:p.Cys463Ser
CA2053233
NM_032974.5:c.1387T>A
CA350293270
NM_032974.5:c.1388G>C