Canonical Allele Identifier: PA218202
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_733822.1:p.Arg89Leu
CA017839
NM_170708.4:c.266G>T