Allele Registry

Canonical Allele Identifier: PA2830327664

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000227837

RCV000597022

RCV001184022

RCV002479935

RCV003998891

RCV004020899

ClinVar Variation:

242002

HGVS (amino-acid)	Matching Registered Transcripts
NP_733821.1:p.Arg419Cys	CA049655 NM_170707.4:c.1255C>T