Allele Registry

Canonical Allele Identifier: PA2830327112

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000592791

RCV001205747

ClinVar Variation:

502071

HGVS (amino-acid)	Matching Registered Transcripts
NP_733821.1:p.Arg298Pro	CA342817795 NM_170707.4:c.893G>C