Canonical Allele Identifier: PA2826659865
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14502

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Glu145Lys
CA018095
NM_001282626.2:c.433G>A