Allele Registry

Canonical Allele Identifier: PA2826443059

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000015621

RCV000057452

RCV000201142

RCV000653857

RCV000814531

ClinVar Variation:

14524

543181

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244303.1:p.Arg137Trp	CA018559 NM_001257374.3:c.409C>T CA658795529 NM_001257374.3:c.408_409delinsTT