Allele Registry

Canonical Allele Identifier: PA2826657803

Gene: LMNA HGNC NCBI

ClinVar Allele:

77669

ClinVar RCV:

RCV000057229

RCV000504480

RCV001218431

ClinVar Variation:

66772

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269553.1:p.Glu280Lys	CA016566 NM_001282624.2:c.838G>A