Canonical Allele Identifier: PA2826659659
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 179969
ClinVar RCV Id: RCV000156772 RCV000768709 RCV001206073
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Arg60Cys
CA017729
NM_001282626.2:c.178C>T