Canonical Allele Identifier: PA218554
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66961

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005563.1:p.Ala318Thr
CA018883
NM_005572.4:c.952G>A