Allele Registry

Canonical Allele Identifier: PA2826660537

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000729830

RCV001862185

ClinVar Variation:

594523

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269555.1:p.Asn456Tyr	CA342822243 NM_001282626.2:c.1366A>T