Canonical Allele Identifier: PA2573237711
Gene: CLCN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 1442624

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004357.3:p.Thr405Met
CA2734191
NM_004366.6:c.1214C>T