Allele Registry

Canonical Allele Identifier: PA2826660536

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000057277

RCV000465598

ClinVar Variation:

66811

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269555.1:p.Asn456Asp	CA017074 NM_001282626.2:c.1366A>G