Canonical Allele Identifier: PA2826657990
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66805

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Asp365Val
CA017008
NM_001282624.2:c.1094A>T