Canonical Allele Identifier: PA2826659102
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14495

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Arg377His
CA016651
NM_001282625.2:c.1130G>A