Canonical Allele Identifier: PA176593
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 163866

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005563.1:p.Arg166Gln
CA018161
NM_005572.4:c.497G>A