Allele Registry

Canonical Allele Identifier: PA2826444095

Gene: LMNA HGNC NCBI

ClinVar Variation Id: 96530

HGVS (amino-acid)	Matching Registered Transcripts
NP_001244303.1:p.Ser513Arg	CA015267 NM_001257374.3:c.1537A>C CA342827516 NM_001257374.3:c.1539C>A CA342827518 NM_001257374.3:c.1539C>G