Allele Registry

Canonical Allele Identifier: PA2826659190

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000057260

RCV000534245

RCV000764982

RCV001191555

RCV002381362

ClinVar Variation:

66797

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269554.1:p.Val415Ile	CA016913 NM_001282625.2:c.1243G>A