Canonical Allele Identifier: PA175463
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 162880

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443068.1:p.Asn434Ser
CA175461
NM_052836.3:c.1301A>G