Canonical Allele Identifier: PA645498275
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 300429
ClinVar RCV Id: RCV000265935 RCV000300732 RCV002520615
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Thr1368Met
CA5544905
NM_022124.6:c.4103C>T