Canonical Allele Identifier: PA137646
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_071407.4:p.Arg3224Trp
CA137645
NM_022124.6:c.9670C>T