Canonical Allele Identifier: PA217741
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14525

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005563.1:p.Glu358Lys
CA016555
NM_005572.4:c.1072G>A