Canonical Allele Identifier: PA217864
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66798

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005563.1:p.Leu421Pro
CA016923
NM_005572.4:c.1262T>C