Allele Registry

Canonical Allele Identifier: PA142586

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000041378

RCV000148604

RCV000619864

RCV000726532

RCV000777745

RCV001086902

RCV001174244

ClinVar Variation:

48092

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244303.1:p.Ile187Val	CA014949 NM_001257374.3:c.559A>G