Canonical Allele Identifier: PA2826658060
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14486

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Arg401Gln
CA014814
NM_001282624.2:c.1202G>A