Canonical Allele Identifier: PA645498703
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 228499
ClinVar RCV Id: RCV000222742 RCV000657978 RCV001275578 RCV002494566
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Asp2218Glu
CA5546141
NM_022124.6:c.6654C>A
CA377155511
NM_022124.6:c.6654C>G