Allele Registry

Canonical Allele Identifier: PA142476

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000041334

RCV000057361

RCV000148601

RCV000617798

RCV000771799

RCV001088263

RCV004541208

ClinVar Variation:

48052

HGVS (amino-acid)	Matching Registered Transcripts
NP_733822.1:p.Gly572Ser	CA014839 NM_170708.4:c.1714G>A