Canonical Allele Identifier: PA2826657871
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66790

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Arg307His
CA016807
NM_001282624.2:c.920G>A