Canonical Allele Identifier: PA261793
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 46000
ClinVar RCV Id: RCV000039235 RCV000763216 RCV001376240 RCV001377826 RCV003473280
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Gly2017Ser
CA261792
NM_022124.6:c.6049G>A