Allele Registry

Canonical Allele Identifier: PA103482

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000057243

RCV003581572

ClinVar Variation:

66782

HGVS (amino-acid)	Matching Registered Transcripts
NP_733821.1:p.Arg386Lys	CA016734 NM_170707.4:c.1157G>A