Canonical Allele Identifier: PA916013533
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14508

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Arg52Pro
CA018038
NM_001282624.2:c.155G>C