Canonical Allele Identifier: PA2826658289
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66928
ClinVar RCV Id: RCV000057449 RCV001048135 RCV002381367
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269554.1:p.Arg25Gly
CA018531
NM_001282625.2:c.73C>G