Canonical Allele Identifier: PA2826658712
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14484

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Glu203Gly
CA018298
NM_001282625.2:c.608A>G