Canonical Allele Identifier: PA124028
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14493

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005563.1:p.Gly465Asp
CA017164
NM_005572.4:c.1394G>A