Canonical Allele Identifier: PA2829970512
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 1407717
ClinVar RCV Id: RCV001937865

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Asp211Glu
CA5543513
NM_022124.6:c.633C>A
CA377112674
NM_022124.6:c.633C>G