Allele Registry

Canonical Allele Identifier: PA2826657715

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV003319250

ClinVar Variation:

2505317

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269553.1:p.Glu243del	CA2580612542 NM_001282624.2:c.729_731del