Allele Registry

Canonical Allele Identifier: PA2826659725

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000015568

RCV000057381

RCV002453264

ClinVar Variation:

14480

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269555.1:p.Leu85Arg	CA017813 NM_001282626.2:c.254T>G