Allele Registry

Canonical Allele Identifier: PA2826660362

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000057235

RCV000503996

RCV000547164

RCV000681569

RCV001089610

RCV002321484

RCV003319170

ClinVar Variation:

14495

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269555.1:p.Arg377His	CA016651 NM_001282626.2:c.1130G>A