Canonical Allele Identifier: PA2829975261
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 2136889
ClinVar RCV Id: RCV003037347
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Gly2912Ser
CA377133032
NM_022124.6:c.8734G>A