Canonical Allele Identifier: PA137339
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 45902
ClinVar RCV Id: RCV000039135 RCV000585571 RCV001106481 RCV001106482 RCV001831659
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Ser944Gly
CA137338
NM_022124.6:c.2830A>G