Canonical Allele Identifier: PA137495
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 45983

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Met1835Ile
CA137494
NM_022124.6:c.5505G>A
CA377146218
NM_022124.6:c.5505G>C
CA377146225
NM_022124.6:c.5505G>T