Canonical Allele Identifier: PA137518
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 45998

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Leu2009His
CA137517
NM_022124.6:c.6026T>A