Canonical Allele Identifier: PA2826093967
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 1297512
ClinVar RCV Id: RCV001723293

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165402.1:p.Met385Leu
CA5543720
NM_001171931.2:c.1153A>T
CA377127415
NM_001171931.2:c.1153A>C