Allele Registry

Canonical Allele Identifier: PA262029

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000182367

RCV000593819

RCV000769727

RCV001071970

RCV001265547

RCV002381325

RCV003235003

RCV003335073

ClinVar Variation:

48098

HGVS (amino-acid)	Matching Registered Transcripts
NP_005563.1:p.Arg331Gln	CA018936 NM_005572.4:c.992G>A