Canonical Allele Identifier: PA2826090755
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 46042

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165401.1:p.Arg3Cys
CA137585
NM_001171930.2:c.7C>T