Allele Registry

Canonical Allele Identifier: PA2826660625

Gene: LMNA HGNC NCBI

ClinVar Variation Id: 2132526

HGVS (amino-acid)	Matching Registered Transcripts
NP_001269555.1:p.Ser507Arg	CA342823116 NM_001282626.2:c.1519A>C CA342823129 NM_001282626.2:c.1521C>A CA342823132 NM_001282626.2:c.1521C>G