Allele Registry

Canonical Allele Identifier: PA2826660267

Gene: LMNA HGNC NCBI

ClinVar Allele:

77655

ClinVar RCV:

RCV000057214

RCV000225878

RCV002426615

RCV002483086

RCV003996492

ClinVar Variation:

66758

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269555.1:p.Arg336Gln	CA016433 NM_001282626.2:c.1007G>A