Canonical Allele Identifier: PA2580449498
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 2159979
ClinVar RCV Id: RCV003073105
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Thr1516Ile
CA377160521
NM_022124.6:c.4547C>T