Canonical Allele Identifier: PA916013559
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 430306

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Ala66Pro
CA342815415
NM_001282624.2:c.196G>C