Canonical Allele Identifier: PA915992065
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 177767
ClinVar RCV Id: RCV000154384 RCV001053772 RCV001102961 RCV001102962 RCV001276918 RCV001375066
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165405.1:p.Gly531Ser
CA180727
NM_001171934.1:c.1591G>A