Canonical Allele Identifier: PA1139758307
Gene: CASP10 HGNC NCBI

Linked Data

ClinVar Variation Id: 963347
ClinVar RCV Id: RCV001796862
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116759.2:p.Asp428His
CA350292482
NM_032977.3:c.1282G>C