Allele Registry

Canonical Allele Identifier: PA124032

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000015585

RCV000057353

RCV001068657

RCV001804734

RCV002399327

RCV003996099

RCV004532363

ClinVar Variation:

14494

HGVS (amino-acid)	Matching Registered Transcripts
NP_733822.1:p.Arg552His	CA020309 NM_170708.4:c.1655G>A