Canonical Allele Identifier: PA2826658287
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66932

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Arg25Pro
CA018579
NM_001282625.2:c.74G>C