Canonical Allele Identifier: PA915992208
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 162956

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165405.1:p.Arg949Gln
CA175533
NM_001171934.1:c.2846G>A