Allele Registry

Canonical Allele Identifier: PA2826657775

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV003532557

RCV004011490

ClinVar Variation:

2773540

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269553.1:p.Arg270Lys	CA048892 NM_001282624.2:c.809G>A