Canonical Allele Identifier: PA218373
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66915

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005563.1:p.Glu203Val
CA018303
NM_005572.4:c.608A>T