Canonical Allele Identifier: PA2741998779
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 2862546
ClinVar RCV Id: RCV003699886

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443068.1:p.His248Tyr
CA377113279
NM_052836.3:c.742C>T