Canonical Allele Identifier: PA2826657421
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66908

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Arg109Trp
CA018245
NM_001282624.2:c.325C>T