Allele Registry

Canonical Allele Identifier: PA2826443425

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000592581

RCV000696116

ClinVar Variation:

498978

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244303.1:p.Glu260Lys	CA342820494 NM_001257374.3:c.778G>A