Canonical Allele Identifier: PA2826659268
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66810

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Arg455Pro
CA017066
NM_001282625.2:c.1364G>C