Allele Registry

Canonical Allele Identifier: PA2826660302

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV002412824

ClinVar Variation:

1781137

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269555.1:p.Gln355dup	CA2580611202 NM_001282626.2:c.1064_1066dup