Canonical Allele Identifier: PA137432
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 45948
ClinVar RCV Id: RCV000039182 RCV001246417 RCV001826571
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Ser1500Thr
CA137431
NM_022124.6:c.4498T>A