Allele Registry

Canonical Allele Identifier: PA2826658151

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000015619

RCV000057331

ClinVar Variation:

14522

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269553.1:p.Ala448Thr	CA017528 NM_001282624.2:c.1342G>A