Canonical Allele Identifier: PA2826660158
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 48090
ClinVar RCV Id: RCV000041376 RCV000505709 RCV000692291 RCV002054813
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Glu290Lys
CA018785
NM_001282626.2:c.868G>A