Canonical Allele Identifier: PA1139693571
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 921469
ClinVar RCV Id: RCV001180909

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.His82Arg
CA342815622
NM_001282624.2:c.245A>G