Canonical Allele Identifier: PA915992057
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 162946
ClinVar RCV Id: RCV000150324 RCV000928676 RCV001108165 RCV001108166 RCV002514890 RCV003389457 RCV004544350
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165405.1:p.Val524Met
CA175522
NM_001171934.1:c.1570G>A