Allele Registry

Canonical Allele Identifier: PA124095

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000015619

RCV000057331

ClinVar Variation:

14522

HGVS (amino-acid)	Matching Registered Transcripts
NP_733821.1:p.Ala529Thr	CA017528 NM_170707.4:c.1585G>A