Canonical Allele Identifier: PA2826659023
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66760

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Glu347Lys
CA016456
NM_001282625.2:c.1039G>A