Canonical Allele Identifier: PA915953879
Gene: CLCN1 HGNC NCBI

Linked Data

ClinVar Variation Id: 447060

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000074.3:p.Asn745Ser
CA4537596
NM_000083.3:c.2234A>G