Allele Registry

Canonical Allele Identifier: PA2826657824

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000592581

RCV000696116

ClinVar Variation:

498978

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269553.1:p.Glu291Lys	CA342820494 NM_001282624.2:c.871G>A