Canonical Allele Identifier: PA916050898
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 228502
ClinVar RCV Id: RCV000223293 RCV001212812 RCV001835729 RCV002478766
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_443068.1:p.Pro251Leu
CA5543528
NM_052836.3:c.752C>T