Canonical Allele Identifier: PA2826281450
Gene: CASP10 HGNC NCBI
ClinVar RCV:
RCV001876676
ClinVar Variation:
1356222
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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