Allele Registry

Canonical Allele Identifier: PA2826659414

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000015571

RCV000057333

ClinVar Variation:

14482

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269554.1:p.Leu530Pro	CA017541 NM_001282625.2:c.1589T>C