Allele Registry

Canonical Allele Identifier: PA2826657771

Gene: LMNA HGNC NCBI

Linked Data - NCBI & NCI

ClinVar Allele:

77659

ClinVar RCV:

RCV000057218

RCV000500548

RCV000653911

RCV000754811

RCV000845011

RCV002504959

RCV003996495

ClinVar Variation:

66762

Amino-acid Alleles

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269553.1:p.Arg268Trp	CA016479 NM_001282624.2:c.802C>T