Allele Registry

Canonical Allele Identifier: PA2826660368

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000015620

RCV000057237

ClinVar Variation:

14523

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269555.1:p.Leu380Ser	CA016670 NM_001282626.2:c.1139T>C