Canonical Allele Identifier: PA137386
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 45925
ClinVar RCV Id: RCV000039158 RCV000968181 RCV001108864 RCV001108865 RCV001272887
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Val1207Met
CA137385
NM_022124.6:c.3619G>A