Canonical Allele Identifier: PA103873
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14502

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Glu145Lys
CA018095
NM_170707.4:c.433G>A