Canonical Allele Identifier: PA916013557
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14502

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Glu64Lys
CA018095
NM_001282624.2:c.190G>A