Canonical Allele Identifier: PA2580103367
Gene: CLCN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2047788

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000074.3:p.Thr874Ser
CA4537755
NM_000083.3:c.2621C>G
CA369653478
NM_000083.3:c.2620A>T