Canonical Allele Identifier: PA137436
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 45950
ClinVar RCV Id: RCV000039184
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Asp1519His
CA137435
NM_022124.6:c.4555G>C