Canonical Allele Identifier: PA645498126
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 420498

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Gly1084Cys
CA16618980
NM_022124.6:c.3250G>T