Canonical Allele Identifier: PA2826284187
Gene: CASP10 HGNC NCBI

Linked Data

ClinVar Variation Id: 333436
ClinVar RCV Id: RCV000334321
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193471.1:p.Gly396Val
CA10612331
NM_001206542.2:c.1187G>T