Allele Registry

Canonical Allele Identifier: PA2826658992

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV001317047

ClinVar Variation:

1017837

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269554.1:p.Glu330Lys	CA342820135 NM_001282625.2:c.988G>A