Canonical Allele Identifier: PA2830329980
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1779689

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Gly559Glu
CA342826667
NM_170708.4:c.1676G>A