Allele Registry

Canonical Allele Identifier: PA2826443355

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV003532557

RCV004011490

ClinVar Variation:

2773540

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244303.1:p.Arg239Lys	CA048892 NM_001257374.3:c.716G>A