Canonical Allele Identifier: PA2826659841
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14508

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Arg133Pro
CA018038
NM_001282626.2:c.398G>C