Canonical Allele Identifier: PA103983
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66806

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733821.1:p.Gly449Asp
CA017024
NM_170707.4:c.1346G>A