Allele Registry

Canonical Allele Identifier: PA2826659038

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV003532557

RCV004011490

ClinVar Variation:

2773540

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269554.1:p.Arg351Lys	CA048892 NM_001282625.2:c.1052G>A