Allele Registry

Canonical Allele Identifier: PA104212

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000015568

RCV000057381

RCV002453264

ClinVar Variation:

14480

HGVS (amino-acid)	Matching Registered Transcripts
NP_733821.1:p.Leu85Arg	CA017813 NM_170707.4:c.254T>G