Allele Registry

Canonical Allele Identifier: PA2826660020

Gene: LMNA HGNC NCBI

ClinVar Allele:

1409306

ClinVar RCV:

RCV001942505

ClinVar Variation:

1364825

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269555.1:p.Arg225Leu	CA342817174 NM_001282626.2:c.674G>T