Allele Registry

Canonical Allele Identifier: PA2826443453

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000015620

RCV000057237

ClinVar Variation:

14523

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244303.1:p.Leu268Ser	CA016670 NM_001257374.3:c.803T>C