Allele Registry

Canonical Allele Identifier: PA2826657780

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV002412824

ClinVar Variation:

1781137

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269553.1:p.Gln274dup	CA2580611202 NM_001282624.2:c.821_823dup