Allele Registry

Canonical Allele Identifier: PA2826658138

Gene: LMNA HGNC NCBI

Linked Data - NCBI & NCI

ClinVar RCV:

RCV000041324

RCV000057323

RCV000182372

RCV000245950

RCV000474372

RCV000678714

RCV001181346

RCV001250579

RCV001330499

RCV003996456

RCV003996716

ClinVar Variation:

48045

200946

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269553.1:p.Gly442Arg	CA017464 NM_001282624.2:c.1324G>A CA017471 NM_001282624.2:c.1324G>C