Canonical Allele Identifier: PA2826659578
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66962
ClinVar RCV Id: RCV000057495 RCV002513742
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Glu33Gly
CA018931
NM_001282626.2:c.98A>G