Canonical Allele Identifier: PA240779
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 194671

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Thr532Met
CA240778
NM_022124.6:c.1595C>T