Allele Registry

Canonical Allele Identifier: PA103587

Gene: LMNA HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

29529

ClinVar RCV:

RCV000015580

RCV000057300

RCV001097055

RCV001097056

RCV001098782

RCV001098783

RCV001098784

RCV001098785

RCV001098786

RCV001098787

RCV001098788

ClinVar Variation:

14490

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_733821.1:p.Arg482Leu	CA017271 NM_170707.4:c.1445G>T