Canonical Allele Identifier: PA137296
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 45879
ClinVar RCV Id: RCV000039112 RCV001042981 RCV001826564 RCV003278657
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Arg546Gln
CA137295
NM_022124.6:c.1637G>A