Canonical Allele Identifier: PA2826092767
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 420498

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165401.1:p.Gly1084Cys
CA16618980
NM_001171930.2:c.3250G>T