Canonical Allele Identifier: PA261954
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 48031

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005563.1:p.Arg377Cys
CA016641
NM_005572.4:c.1129C>T