Canonical Allele Identifier: PA2826096447
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 1984030
ClinVar RCV Id: RCV002756717
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165404.1:p.Ala111Ser
CA377158531
NM_001171933.1:c.331G>T