Allele Registry

Canonical Allele Identifier: PA2826658040

Gene: LMNA HGNC NCBI

ClinVar Allele:

77721

ClinVar RCV:

RCV000057292

RCV002390204

RCV002514282

ClinVar Variation:

66824

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269553.1:p.Arg390Gly	CA017206 NM_001282624.2:c.1168C>G