Canonical Allele Identifier: PA217870
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66799

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005563.1:p.Ala43Thr
CA016942
NM_005572.4:c.127G>A