Canonical Allele Identifier: PA2826281639
Gene: CASP10 HGNC NCBI

Linked Data

ClinVar Variation Id: 333431

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001221.2:p.Ser250Arg
CA2053088
NM_001230.5:c.750C>A
CA350286539
NM_001230.5:c.748A>C
CA350286558
NM_001230.5:c.750C>G