Canonical Allele Identifier: PA137412
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 45936
ClinVar RCV Id: RCV000039170 RCV000892452 RCV001106789 RCV001106790 RCV001831665 RCV004534830
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165401.1:p.Arg1349Cys
CA137411
NM_001171930.2:c.4045C>T