Allele Registry

Canonical Allele Identifier: PA2826657798

Gene: LMNA HGNC NCBI

ClinVar Allele:

29564

ClinVar RCV:

RCV000015622

RCV000015623

RCV000057227

RCV000470514

RCV000502108

RCV001420791

ClinVar Variation:

14525

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269553.1:p.Glu277Lys	CA016555 NM_001282624.2:c.829G>A