Allele Registry

Canonical Allele Identifier: PA2826659392

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000540642

RCV001213240

ClinVar Variation:

476824

943114

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269554.1:p.Trp520Arg	CA342823343 NM_001282625.2:c.1558T>C CA342823345 NM_001282625.2:c.1558T>A