Canonical Allele Identifier: PA2826094022
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 1368507
ClinVar RCV Id: RCV001894669
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165402.1:p.Thr423Ser
CA377127834
NM_001171931.2:c.1267A>T
CA377127836
NM_001171931.2:c.1268C>G