Canonical Allele Identifier: PA2826658194
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 2773548

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Thr467Ala
CA342825486
NM_001282624.2:c.1399A>G