Canonical Allele Identifier: PA137457
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 45962
ClinVar RCV Id: RCV000039196 RCV000317490 RCV000372199 RCV000723750 RCV001273552 RCV002513528
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Arg1684Cys
CA137456
NM_022124.6:c.5050C>T