Allele Registry

Canonical Allele Identifier: PA103883

Gene: LMNA HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

29543

ClinVar RCV:

RCV000015598

RCV000057409

RCV000211788

RCV000687241

RCV001170451

RCV003318333

RCV004018635

ClinVar Variation:

14504

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_733821.1:p.Glu161Lys	CA018140 NM_170707.4:c.481G>A