Canonical Allele Identifier: PA185014
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 179731
ClinVar RCV Id: RCV000766640 RCV001106863 RCV000778901 RCV002492595 RCV001835699 RCV003474814
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Ile1469Val
CA185013
NM_022124.6:c.4405A>G