Canonical Allele Identifier: PA2826659143
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 959791

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Thr394Ile
CA049322
NM_001282625.2:c.1181C>T