Allele Registry

Canonical Allele Identifier: PA142587

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000041378

RCV000148604

RCV000619864

RCV000726532

RCV000777745

RCV001086902

RCV001174244

ClinVar Variation:

48092

HGVS (amino-acid)	Matching Registered Transcripts
NP_005563.1:p.Ile299Val	CA014949 NM_005572.4:c.895A>G