Canonical Allele Identifier: PA137388
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 4927

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Thr1209Ala
CA137387
NM_022124.6:c.3625A>G