Canonical Allele Identifier: PA2826094047
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 162880

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165402.1:p.Asn434Ser
CA175461
NM_001171931.2:c.1301A>G