Canonical Allele Identifier: PA658818882
Gene: CASP10 HGNC NCBI

Linked Data

ClinVar Variation Id: 535757
ClinVar RCV Id: RCV001796759
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_116759.2:p.Ala307Asp
CA350287126
NM_032977.3:c.920C>A