Canonical Allele Identifier: PA2826431784
Gene: CLCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 429943

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243873.1:p.Gly175Asp
CA412037184
NM_001256944.2:c.524G>A