Canonical Allele Identifier: PA1139752605
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 877825

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Arg1588Trp
CA5545144
NM_022124.6:c.4762C>T