Canonical Allele Identifier: PA1139751040
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 958298
ClinVar RCV Id: RCV001231439

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443068.1:p.Asp430Asn
CA5543753
NM_052836.3:c.1288G>A