Canonical Allele Identifier: PA2826443671
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66808

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244303.1:p.Arg341Pro
CA017039
NM_001257374.3:c.1022G>C