Allele Registry

Canonical Allele Identifier: PA2826658178

Gene: LMNA HGNC NCBI

Linked Data

ClinVar RCV:

RCV000057344

RCV000221013

RCV000230467

RCV000246865

RCV001262710

RCV001836636

RCV003335086

RCV004018989

ClinVar Variation:

66860

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269553.1:p.Arg460His	CA017621 NM_001282624.2:c.1379G>A