Canonical Allele Identifier: PA137482
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 45976
ClinVar RCV Id: RCV000039211 RCV000124201 RCV001104090 RCV001274892 RCV001533705 RCV002504904
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Asp1806Glu
CA137481
NM_022124.6:c.5418C>G
CA377144757
NM_022124.6:c.5418C>A