Allele Registry

Canonical Allele Identifier: PA2826658141

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000015569

RCV000015570

RCV000057327

RCV000700159

RCV001375641

RCV004018633

ClinVar Variation:

14481

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269553.1:p.Arg446Pro	CA017498 NM_001282624.2:c.1337G>C