Canonical Allele Identifier: PA175505
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 162932

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Asp2219Asn
CA175504
NM_022124.6:c.6655G>A