Canonical Allele Identifier: PA137353
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 45908
ClinVar RCV Id: RCV000039141 RCV000839197 RCV001105453 RCV001105454 RCV001272552 RCV001328026 RCV004534828
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165402.1:p.Gly1025Asp
CA137352
NM_001171931.2:c.3074G>A