Canonical Allele Identifier: PA915992021
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 46045
ClinVar RCV Id: RCV000039281 RCV000725935 RCV001108161 RCV001108162 RCV001276044
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165405.1:p.Val483Leu
CA137590
NM_001171934.1:c.1447G>C
CA377162493
NM_001171934.1:c.1447G>T