Allele Registry

Canonical Allele Identifier: PA2826443363

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV002412824

ClinVar Variation:

1781137

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244303.1:p.Gln243dup	CA2580611202 NM_001257374.3:c.728_730dup