Canonical Allele Identifier: PA180728
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 177767
ClinVar RCV Id: RCV000154384 RCV001053772 RCV001102961 RCV001102962 RCV001276918 RCV001375066
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Gly2771Ser
CA180727
NM_022124.6:c.8311G>A