Allele Registry

Canonical Allele Identifier: PA645457878

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000500844

RCV000697810

RCV000705726

ClinVar Variation:

435773

581796

HGVS (amino-acid)	Matching Registered Transcripts
NP_733822.1:p.Leu530Phe	CA342823527 NM_170708.4:c.1588C>T CA891842720 NM_170708.4:c.1587_1588delinsCT