Allele Registry

Canonical Allele Identifier: PA2826658228

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000057045

RCV000790249

RCV001176130

RCV001854169

RCV002504958

RCV003996491

ClinVar Variation:

66611

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269553.1:p.Arg490Cys	CA017701 NM_001282624.2:c.1468C>T