Canonical Allele Identifier: PA2580449323
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 2167747
ClinVar RCV Id: RCV003092201
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Gly1118Val
CA5544557
NM_022124.6:c.3353G>T