Canonical Allele Identifier: PA2826094862
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 522662
ClinVar RCV Id: RCV000625802
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165402.1:p.Asp804Asn
CA377137461
NM_001171931.2:c.2410G>A