Allele Registry

Canonical Allele Identifier: PA2826442799

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000015598

RCV000057409

RCV000211788

RCV000687241

RCV001170451

RCV003318333

RCV004018635

ClinVar Variation:

14504

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244303.1:p.Glu49Lys	CA018140 NM_001257374.3:c.145G>A