Allele Registry

Canonical Allele Identifier: PA2826657895

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000057256

RCV000550366

RCV001184773

RCV002336207

RCV003996500

ClinVar Variation:

66794

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269553.1:p.Arg318His	CA016854 NM_001282624.2:c.953G>A