Canonical Allele Identifier: PA137388
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 4927
ClinVar RCV Id: RCV000005210 RCV000039159 RCV000086973 RCV000217147 RCV000263856 RCV000787989 RCV002490319
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Thr1209Ala
CA137387
NM_022124.6:c.3625A>G