Canonical Allele Identifier: PA2826443486
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66790

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244303.1:p.Arg276His
CA016807
NM_001257374.3:c.827G>A