Canonical Allele Identifier: PA2826657803
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66772
ClinVar RCV Id: RCV000057229 RCV000504480 RCV001218431
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Glu280Lys
CA016566
NM_001282624.2:c.838G>A