Canonical Allele Identifier: PA915992084
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 100590
ClinVar RCV Id: RCV000086978
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165405.1:p.Lys564Arg
CA228930
NM_001171934.1:c.1691A>G