Canonical Allele Identifier: PA218079
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 14482

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Leu530Pro
CA017541
NM_170708.4:c.1589T>C