Allele Registry

Canonical Allele Identifier: PA2826658104

Gene: LMNA HGNC NCBI

ClinVar Variation Id: 2132526

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269553.1:p.Ser426Arg	CA342823116 NM_001282624.2:c.1276A>C CA342823129 NM_001282624.2:c.1278C>A CA342823132 NM_001282624.2:c.1278C>G