Canonical Allele Identifier: PA645497722
Gene: CDH23 HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Asp228Val
CA16609568
NM_022124.6:c.683A>T