Canonical Allele Identifier: PA2826101161
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 162956

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165407.1:p.Arg86Gln
CA175533
NM_001171936.1:c.257G>A