Allele Registry

Canonical Allele Identifier: PA2826443296

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000182367

RCV000593819

RCV000769727

RCV001071970

RCV001265547

RCV002381325

RCV003235003

RCV003335073

ClinVar Variation:

48098

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244303.1:p.Arg219Gln	CA018936 NM_001257374.3:c.656G>A