Allele Registry

Canonical Allele Identifier: PA217752

Gene: LMNA HGNC NCBI

ClinVar Allele:

77669

ClinVar RCV:

RCV000057229

RCV000504480

RCV001218431

ClinVar Variation:

66772

HGVS (amino-acid)	Matching Registered Transcripts
NP_005563.1:p.Glu361Lys	CA016566 NM_005572.4:c.1081G>A