Canonical Allele Identifier: PA137367
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 45914
ClinVar RCV Id: RCV000039147 RCV000280070 RCV000406184 RCV000487639 RCV004528192 RCV003242971
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Val1111Ile
CA137366
NM_022124.6:c.3331G>A