Canonical Allele Identifier: PA253333
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 4922

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Asp2148Asn
CA253332
NM_022124.6:c.6442G>A