Canonical Allele Identifier: PA2826076854
Gene: CLCN2 HGNC NCBI

Linked Data

ClinVar Variation Id: 772363

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001164558.1:p.Pro381Ala
CA2734222
NM_001171087.2:c.1141C>G