Canonical Allele Identifier: PA137508
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 45992
ClinVar RCV Id: RCV000039227 RCV000271728 RCV000325842 RCV000905205 RCV001275564 RCV004528194
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Arg1918Gln
CA137507
NM_022124.6:c.5753G>A