Canonical Allele Identifier: PA182071
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 178302
ClinVar RCV Id: RCV000155046 RCV001051031 RCV001275940
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Ala781Thr
CA182070
NM_022124.6:c.2341G>A