Canonical Allele Identifier: PA2826094006
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 839894
ClinVar RCV Id: RCV001041755
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165402.1:p.Ile411Val
CA377127762
NM_001171931.2:c.1231A>G