Allele Registry

Canonical Allele Identifier: PA2826443833

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000540642

RCV001213240

ClinVar Variation:

476824

943114

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244303.1:p.Trp408Arg	CA342823343 NM_001257374.3:c.1222T>C CA342823345 NM_001257374.3:c.1222T>A