Allele Registry

Canonical Allele Identifier: PA2826657930

Gene: LMNA HGNC NCBI

ClinVar Allele:

77694

ClinVar RCV:

RCV000057260

RCV000534245

RCV000764982

RCV001191555

RCV002381362

ClinVar Variation:

66797

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269553.1:p.Val334Ile	CA016913 NM_001282624.2:c.1000G>A