Canonical Allele Identifier: PA2826659109
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1480633
ClinVar RCV Id: RCV002000340

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Glu381Lys
CA342820607
NM_001282625.2:c.1141G>A