Canonical Allele Identifier: PA2573185437
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 1677240
ClinVar RCV Id: RCV002223098

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165405.1:p.Ile429Val
CA377162141
NM_001171934.1:c.1285A>G