Canonical Allele Identifier: PA2826281450
Gene: CASP10 HGNC NCBI

Linked Data

ClinVar Variation Id: 1356222
ClinVar RCV Id: RCV001876676
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001221.2:p.Arg21Cys
CA2052768
NM_001230.5:c.61C>T