Canonical Allele Identifier: PA2826443865
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66850

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244303.1:p.Thr416Arg
CA017510
NM_001257374.3:c.1247C>G