Allele Registry

Canonical Allele Identifier: PA218441

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000015621

RCV000057452

RCV000201142

RCV000653857

RCV000814531

ClinVar Variation:

14524

543181

HGVS (amino-acid)	Matching Registered Transcripts
NP_733822.1:p.Arg249Trp	CA018559 NM_170708.4:c.745C>T CA658795529 NM_170708.4:c.744_745delinsTT