Canonical Allele Identifier: PA2580156877
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 2038562
ClinVar RCV Id: RCV002895050
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165405.1:p.Ala565Pro
CA377131493
NM_001171934.1:c.1693G>C