Allele Registry

Canonical Allele Identifier: PA2826658155

Gene: LMNA HGNC NCBI

ClinVar Allele:

427654

556967

ClinVar RCV:

RCV000500844

RCV000697810

RCV000705726

ClinVar Variation:

435773

581796

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269553.1:p.Leu449Phe	CA342823527 NM_001282624.2:c.1345C>T CA891842720 NM_001282624.2:c.1344_1345delinsCT