Canonical Allele Identifier: PA645498885
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 300465

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Asp2942Asn
CA5546760
NM_022124.6:c.8824G>A