Canonical Allele Identifier: PA2826658776
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66925

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Gly232Glu
CA018472
NM_001282625.2:c.695G>A