Allele Registry

Canonical Allele Identifier: PA2830326476

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV001307001

RCV004005039

ClinVar Variation:

1009498

HGVS (amino-acid)	Matching Registered Transcripts
NP_733821.1:p.Ala147Thr	CA053436 NM_170707.4:c.439G>A