Allele Registry

Canonical Allele Identifier: PA2826658334

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV003019110

RCV003140304

ClinVar Variation:

2098082

2431242

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269554.1:p.Asn39Lys	CA342807688 NM_001282625.2:c.117T>A CA342807691 NM_001282625.2:c.117T>G