Canonical Allele Identifier: PA2826443392
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66772

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244303.1:p.Glu249Lys
CA016566
NM_001257374.3:c.745G>A