Allele Registry

Canonical Allele Identifier: PA2830326986

Gene: LMNA HGNC NCBI

ClinVar Allele:

427648

ClinVar RCV:

RCV000503745

RCV001382395

ClinVar Variation:

435769

HGVS (amino-acid)	Matching Registered Transcripts
NP_733821.1:p.Ala278Pro	CA342817513 NM_170707.4:c.832G>C