Canonical Allele Identifier: PA2826659558
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 285468
ClinVar RCV Id: RCV000380269 RCV000809047 RCV002298563
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Arg28Gln
CA10605120
NM_001282626.2:c.83G>A