Canonical Allele Identifier: PA2826659829
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1427183
ClinVar RCV Id: RCV001945851

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Leu127Pro
CA342815093
NM_001282626.2:c.380T>C