Allele Registry

Canonical Allele Identifier: PA2826659802

Gene: LMNA HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000041346

RCV000324940

RCV000653882

RCV000853426

RCV001007778

RCV001098092

RCV001098093

RCV001098094

RCV001098095

RCV001099881

RCV001099882

RCV001182267

RCV002336155

RCV003996462

ClinVar Variation:

48063

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269555.1:p.Lys117Arg	CA017949 NM_001282626.2:c.350A>G