Allele Registry

Canonical Allele Identifier: PA2826443291

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV001317047

ClinVar Variation:

1017837

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244303.1:p.Glu218Lys	CA342820135 NM_001257374.3:c.652G>A