Canonical Allele Identifier: PA137461
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 45964
ClinVar RCV Id: RCV000039198 RCV000281904 RCV000318225 RCV000844910 RCV000912043 RCV001272904
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Met1689Thr
CA137460
NM_022124.6:c.5066T>C