Canonical Allele Identifier: PA218450
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66932

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005563.1:p.Arg25Pro
CA018579
NM_005572.4:c.74G>C