Canonical Allele Identifier: PA306168
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 200932
ClinVar RCV Id: RCV000182354 RCV000223737 RCV000852405 RCV000707542
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_733822.1:p.Glu115Val
CA017931
NM_170708.4:c.344A>T