Allele Registry

Canonical Allele Identifier: PA2826658356

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000057281

RCV001230439

ClinVar Variation:

66815

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269554.1:p.Ile46Val	CA017105 NM_001282625.2:c.136A>G