Canonical Allele Identifier: PA137597
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 46048
ClinVar RCV Id: RCV000039284 RCV001243714 RCV001276919 RCV002513536
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Val2803Ile
CA137596
NM_022124.6:c.8407G>A