Allele Registry

Canonical Allele Identifier: PA2580509452

Gene: LMNA HGNC NCBI

ClinVar Variation Id: 2132526

HGVS (amino-acid)	Matching Registered Transcripts
NP_733822.1:p.Ser507Arg	CA342823116 NM_170708.4:c.1519A>C CA342823129 NM_170708.4:c.1521C>A CA342823132 NM_170708.4:c.1521C>G