Canonical Allele Identifier: PA217925
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66808

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Arg453Pro
CA017039
NM_170708.4:c.1358G>C