Canonical Allele Identifier: PA2826659974
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66915

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Glu203Val
CA018303
NM_001282626.2:c.608A>T