Allele Registry

Canonical Allele Identifier: PA2826443872

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000500844

RCV000697810

RCV000705726

ClinVar Variation:

435773

581796

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244303.1:p.Leu418Phe	CA342823527 NM_001257374.3:c.1252C>T CA891842720 NM_001257374.3:c.1251_1252delinsCT