Canonical Allele Identifier: PA2826283972
Gene: CASP10 HGNC NCBI

Linked Data

ClinVar Variation Id: 333416
ClinVar RCV Id: RCV000288669
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001193471.1:p.Lys17Glu
CA2052766
NM_001206542.2:c.49A>G