Allele Registry

Canonical Allele Identifier: PA2826659065

Gene: LMNA HGNC NCBI

ClinVar Variation Id: 66772

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269554.1:p.Glu361Lys	CA016566 NM_001282625.2:c.1081G>A