Canonical Allele Identifier: PA137438
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 45951
ClinVar RCV Id: RCV000039185 RCV001047099 RCV001826572 RCV002513527
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Val154Met
CA137437
NM_022124.6:c.460G>A