Canonical Allele Identifier: PA137542
Gene: CDH23 HGNC NCBI

Linked Data

ClinVar Variation Id: 46014

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_071407.4:p.Pro2205Leu
CA137541
NM_022124.6:c.6614C>T