Canonical Allele Identifier: PA2826099249
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 3141220
ClinVar RCV Id: RCV004428076

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165405.1:p.Val563Phe
CA377131482
NM_001171934.1:c.1687G>T