Allele Registry

Canonical Allele Identifier: PA2826657769

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV003743173

ClinVar Variation:

2860240

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269553.1:p.Arg268Gln	CA342820264 NM_001282624.2:c.803G>A