Allele Registry

Canonical Allele Identifier: PA2826659407

Gene: LMNA HGNC NCBI

ClinVar Allele:

77747

ClinVar RCV:

RCV000057329

RCV000472329

RCV000499741

RCV001814041

RCV003483458

ClinVar Variation:

66850

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269554.1:p.Thr528Arg	CA017510 NM_001282625.2:c.1583C>G