Canonical Allele Identifier: PA2826657614
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 435769

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Ala197Pro
CA342817513
NM_001282624.2:c.589G>C