Canonical Allele Identifier: PA2826281813
Gene: CASP10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1014291
ClinVar RCV Id: RCV001796873

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001221.2:p.Ser386Gly
CA350292522
NM_001230.5:c.1156A>G