Canonical Allele Identifier: PA2826093716
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 4928

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165402.1:p.Pro240Leu
CA253338
NM_001171931.2:c.719C>T