Canonical Allele Identifier: PA2826659782
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1513940
ClinVar RCV Id: RCV002018518
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Glu111Gly
CA342808848
NM_001282626.2:c.332A>G