Allele Registry

Canonical Allele Identifier: PA137495

Gene: CDH23 HGNC NCBI

ClinVar Variation Id: 45983

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