Canonical Allele Identifier: PA184256
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 179352
ClinVar RCV Id: RCV000156141 RCV000724950 RCV001275568
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Ser2033Leu
CA184255
NM_022124.6:c.6098C>T