Canonical Allele Identifier: PA175462
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 162880

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Asn434Ser
CA175461
NM_022124.6:c.1301A>G