Canonical Allele Identifier: PA2826092748
Gene: CDH23 HGNC NCBI
ClinVar RCV:
RCV002636527
ClinVar Variation:
2188393
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165401.1:p.Gly1076Ser
CA377143963
NM_001171930.2:c.3226G>A