Canonical Allele Identifier: PA916050923
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 4929

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443068.1:p.Arg301Gln
CA239352
NM_052836.3:c.902G>A