Canonical Allele Identifier: PA915953613
Gene: CLCN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 432168

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000074.3:p.Trp303Gly
CA369641598
NM_000083.3:c.907T>G