Canonical Allele Identifier: PA217770
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14495

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Arg377His
CA016651
NM_170708.4:c.1130G>A