Canonical Allele Identifier: PA2826092781
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 166812

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165401.1:p.Ile1101Val
CA233645
NM_001171930.2:c.3301A>G