Canonical Allele Identifier: PA2826444098
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 518817

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001244303.1:p.Ser513Pro
CA658795542
NM_001257374.3:c.1537_1538delinsCC