Canonical Allele Identifier: PA137304
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 45883
ClinVar RCV Id: RCV000039116 RCV000285125 RCV000340118 RCV000882018 RCV001275932 RCV003389446 RCV004528188
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Ala605Val
CA137303
NM_022124.6:c.1814C>T