Allele Registry

Canonical Allele Identifier: PA2826660565

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000755017

ClinVar Variation:

617763

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269555.1:p.Arg471Pro	CA342822531 NM_001282626.2:c.1412G>C