Allele Registry

Canonical Allele Identifier: PA2826659876

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000208276

RCV000536399

RCV000611547

RCV002327072

ClinVar Variation:

222692

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269555.1:p.Thr150Ala	CA088193 NM_001282626.2:c.448A>G