Canonical Allele Identifier: PA2826601650
Gene: CLCN5 HGNC NCBI

Linked Data

ClinVar Variation Id: 368485

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269092.1:p.Val556Met
CA10413928
NM_001282163.2:c.1666G>A