Allele Registry

Canonical Allele Identifier: PA2829602778

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000529491

RCV000785916

ClinVar Variation:

476837

HGVS (amino-acid)	Matching Registered Transcripts
NP_005563.1:p.Lys32Glu	CA342807424 NM_005572.4:c.94A>G