Allele Registry

Canonical Allele Identifier: PA103278

Gene: LMNA HGNC NCBI

ClinVar Allele:

29552

ClinVar RCV:

RCV000015608

RCV000057332

RCV002399329

RCV002467496

RCV003234906

ClinVar Variation:

14513

HGVS (amino-acid)	Matching Registered Transcripts
NP_733821.1:p.Ala529Val	CA017534 NM_170707.4:c.1586C>T