Allele Registry

Canonical Allele Identifier: PA103683

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000057341

RCV000823221

RCV004017361

ClinVar Variation:

66859

HGVS (amino-acid)	Matching Registered Transcripts
NP_733821.1:p.Arg541Ser	CA017601 NM_170707.4:c.1621C>A