Allele Registry

Canonical Allele Identifier: PA217987

Gene: LMNA HGNC NCBI

ClinVar Allele:

77721

ClinVar RCV:

RCV000057292

RCV002390204

RCV002514282

ClinVar Variation:

66824

HGVS (amino-acid)	Matching Registered Transcripts
NP_005563.1:p.Arg471Gly	CA017206 NM_005572.4:c.1411C>G