Canonical Allele Identifier: PA2826283882
Gene: CASP10 HGNC NCBI

Linked Data

ClinVar Variation Id: 21728

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193453.1:p.Tyr379Cys
CA342419
NM_001206524.2:c.1136A>G