Canonical Allele Identifier: PA2826657450
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14484

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Glu122Gly
CA018298
NM_001282624.2:c.365A>G