Allele Registry

Canonical Allele Identifier: PA2829604059

Gene: LMNA HGNC NCBI

ClinVar Allele:

447237

930071

ClinVar RCV:

RCV000540642

RCV001213240

ClinVar Variation:

476824

943114

HGVS (amino-acid)	Matching Registered Transcripts
NP_005563.1:p.Trp520Arg	CA342823343 NM_005572.4:c.1558T>C CA342823345 NM_005572.4:c.1558T>A