Allele Registry

Canonical Allele Identifier: PA2830327852

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000729830

RCV001862185

ClinVar Variation:

594523

HGVS (amino-acid)	Matching Registered Transcripts
NP_733821.1:p.Asn456Tyr	CA342822243 NM_170707.4:c.1366A>T