Canonical Allele Identifier: PA2829970524
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 1016579
ClinVar RCV Id: RCV001315602
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Ile224Val
CA377112782
NM_022124.6:c.670A>G