Canonical Allele Identifier: PA137572
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 46032
ClinVar RCV Id: RCV000039268 RCV000725960 RCV000763667 RCV001108081 RCV001108080 RCV001276040
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Glu2490Lys
CA137571
NM_022124.6:c.7468G>A