Canonical Allele Identifier: PA2826283893
Gene: CASP10 HGNC NCBI

Linked Data

ClinVar Variation Id: 2948944
ClinVar RCV Id: RCV003801670
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193453.1:p.Lys401Glu
CA2053235
NM_001206524.2:c.1201A>G