Allele Registry

Canonical Allele Identifier: PA2826659004

Gene: LMNA HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

45135

ClinVar RCV:

RCV000030145

RCV000182368

RCV000546102

RCV000620788

RCV000721960

RCV000844672

RCV000845456

RCV000852407

RCV001196390

RCV002477025

RCV003149579

RCV003492303

RCV004532421

ClinVar Variation:

36473

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269554.1:p.Arg335Trp	CA016426 NM_001282625.2:c.1003C>T