Canonical Allele Identifier: PA2826443058
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 48077

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244303.1:p.Arg137Gly
CA018552
NM_001257374.3:c.409C>G