Canonical Allele Identifier: PA218559
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66962

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005563.1:p.Glu33Gly
CA018931
NM_005572.4:c.98A>G