Canonical Allele Identifier: PA133608
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 44114
ClinVar RCV Id: RCV000037090 RCV000513678 RCV001105079 RCV001105080 RCV001544539 RCV001826559
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165403.1:p.Ala366Thr
CA133607
NM_001171932.2:c.1096G>A