Canonical Allele Identifier: PA218564
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66963

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005563.1:p.Arg331Pro
CA018942
NM_005572.4:c.992G>C