Canonical Allele Identifier: PA2826283888
Gene: CASP10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1494185
ClinVar RCV Id: RCV001987054

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193453.1:p.Val385Ala
CA2053229
NM_001206524.2:c.1154T>C