Canonical Allele Identifier: PA915992013
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 300459

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165405.1:p.Asp427His
CA5546501
NM_001171934.1:c.1279G>C