Allele Registry

Canonical Allele Identifier: PA2826659747

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000472865

RCV000598315

RCV001524820

RCV002436430

RCV002489054

RCV003387849

RCV004000799

ClinVar Variation:

408995

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269555.1:p.Lys97Thr	CA16609882 NM_001282626.2:c.290A>C