Allele Registry

Canonical Allele Identifier: PA2826659762

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000622678

RCV001376156

RCV003133407

ClinVar Variation:

520647

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269555.1:p.Leu102Pro	CA342808708 NM_001282626.2:c.305T>C