Canonical Allele Identifier: PA2829975068
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 3141220
ClinVar RCV Id: RCV004428076
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Val2803Phe
CA377131482
NM_022124.6:c.8407G>T