Allele Registry

Canonical Allele Identifier: PA2826659733

Gene: LMNA HGNC NCBI

ClinVar Allele:

77781

ClinVar RCV:

RCV000057383

RCV000462640

ClinVar Variation:

66884

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269555.1:p.Arg89Leu	CA017839 NM_001282626.2:c.266G>T