Allele Registry

Canonical Allele Identifier: PA2826659330

Gene: LMNA HGNC NCBI

ClinVar RCV:

RCV000057301

RCV000057302

RCV000193901

ClinVar Variation:

66828

66829

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269554.1:p.Lys486Asn	CA017278 NM_001282625.2:c.1458G>C CA017283 NM_001282625.2:c.1458G>T