Allele Registry

Canonical Allele Identifier: PA2826443684

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000729830

RCV001862185

ClinVar Variation:

594523

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244303.1:p.Asn344Tyr	CA342822243 NM_001257374.3:c.1030A>T