Allele Registry

Canonical Allele Identifier: PA2826657976

Gene: LMNA HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

29559

ClinVar RCV:

RCV000015617

RCV000057268

RCV000552191

RCV001172618

RCV001186220

RCV001264435

RCV002381252

RCV003996102

ClinVar Variation:

14520

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269553.1:p.Val359Met	CA016999 NM_001282624.2:c.1075G>A