Canonical Allele Identifier: PA645385579
Gene: CLCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 429943

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001821.2:p.Gly269Asp
CA412037184
NM_001830.3:c.806G>A