Canonical Allele Identifier: PA2826657496
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 952652

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Thr143Ile
CA342817171
NM_001282624.2:c.428C>T