Canonical Allele Identifier: PA2826100526
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 162957

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165406.1:p.Arg103His
CA175535
NM_001171935.1:c.308G>A