Canonical Allele Identifier: PA2741907376
Gene: CLCN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2719668
ClinVar RCV Id: RCV003553719

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004357.3:p.Pro381Thr
CA355453513
NM_004366.6:c.1141C>A