Canonical Allele Identifier: PA2826657733
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66963

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Arg250Pro
CA018942
NM_001282624.2:c.749G>C