Canonical Allele Identifier: PA2826658031
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14493

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Gly384Asp
CA017164
NM_001282624.2:c.1151G>A