Canonical Allele Identifier: PA2829970837
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 1368507
ClinVar RCV Id: RCV001894669

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Thr423Ser
CA377127834
NM_022124.6:c.1267A>T
CA377127836
NM_022124.6:c.1268C>G