Canonical Allele Identifier: PA915991926
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 46078
ClinVar RCV Id: RCV000039315 RCV000286542 RCV000341398 RCV000725356 RCV001272665 RCV004528199
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001165404.1:p.Arg984Trp
CA137645
NM_001171933.1:c.2950C>T