Canonical Allele Identifier: PA2826091211
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 4928
ClinVar RCV Id: RCV000005211 RCV001261012 RCV001106128 RCV001205177 RCV002476931 RCV001831515 RCV003472978
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165401.1:p.Pro240Leu
CA253338
NM_001171930.2:c.719C>T