Canonical Allele Identifier: PA2826100496
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 162956

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165406.1:p.Arg86Gln
CA175533
NM_001171935.1:c.257G>A