Canonical Allele Identifier: PA137506
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 45991
ClinVar RCV Id: RCV000039226 RCV001241540 RCV001375123 RCV001826575
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Arg1912Trp
CA137505
NM_022124.6:c.5734C>T