Canonical Allele Identifier: PA103489
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66790

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Arg388His
CA016807
NM_170707.4:c.1163G>A