Canonical Allele Identifier: PA103528
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66808

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Arg453Pro
CA017039
NM_170707.4:c.1358G>C