Allele Registry

Canonical Allele Identifier: PA2826659986

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000015588

RCV000057433

ClinVar Variation:

66918

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269555.1:p.Lys208del	CA018324 NM_001282626.2:c.624_626del