Canonical Allele Identifier: PA137284
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 45873
ClinVar RCV Id: RCV000039106 RCV001103252 RCV001103251 RCV001288115
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Thr491Ile
CA137283
NM_022124.6:c.1472C>T