Canonical Allele Identifier: PA2826281442
Gene: CASP10 HGNC NCBI

Linked Data

ClinVar Variation Id: 333415

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001221.2:p.His7Arg
CA2052764
NM_001230.5:c.20A>G