Canonical Allele Identifier: PA2826098670
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 446449
ClinVar RCV Id: RCV000515741
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165405.1:p.Glu198Lys
CA377159510
NM_001171934.1:c.592G>A