Allele Registry

Canonical Allele Identifier: PA2826658611

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV001307001

RCV004005039

ClinVar Variation:

1009498

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269554.1:p.Ala147Thr	CA053436 NM_001282625.2:c.439G>A