Canonical Allele Identifier: PA2826432070
Gene: CLCN4 HGNC NCBI

Linked Data

ClinVar Variation Id: 209116

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001243873.1:p.Arg624Trp
CA10575780
NM_001256944.2:c.1870C>T