Allele Registry

Canonical Allele Identifier: PA262012

Gene: LMNA HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000041379

RCV000057489

RCV000560270

RCV000769726

RCV001000784

RCV001251293

RCV001775075

RCV002371856

RCV004541210

ClinVar Variation:

48093

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_005563.1:p.Glu317Lys	CA018878 NM_005572.4:c.949G>A