Canonical Allele Identifier: PA2826092812
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 45917
ClinVar RCV Id: RCV000039150 RCV001103614 RCV000965142 RCV001103613 RCV001831660
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165401.1:p.Leu1122Val
CA137372
NM_001171930.2:c.3364T>G