Canonical Allele Identifier: PA645497688
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 228491

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Asp127Gly
CA10576804
NM_022124.6:c.380A>G