Canonical Allele Identifier: PA2829602722
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 2140137

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005563.1:p.Ala9Thr
CA342806038
NM_005572.4:c.25G>A