Canonical Allele Identifier: PA2826659255
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66806

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Gly449Asp
CA017024
NM_001282625.2:c.1346G>A