Allele Registry

Canonical Allele Identifier: PA103579

Gene: LMNA HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

29525

ClinVar RCV:

RCV000015575

RCV000041318

RCV000057299

RCV000190399

RCV000459624

RCV000754814

RCV000763258

RCV001179839

RCV001822996

RCV002390111

RCV004532361

ClinVar Variation:

14486

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_733821.1:p.Arg482Gln	CA014814 NM_170707.4:c.1445G>A