Allele Registry

Canonical Allele Identifier: PA218170

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000057373

ClinVar Variation:

66876

HGVS (amino-acid)	Matching Registered Transcripts
NP_733821.1:p.Arg644Ser	CA015174 NM_170707.4:c.1930C>A