Canonical Allele Identifier: PA2826659733
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66884
ClinVar RCV Id: RCV000057383 RCV000462640
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Arg89Leu
CA017839
NM_001282626.2:c.266G>T