Canonical Allele Identifier: PA2826659718
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 66882
ClinVar RCV Id: RCV000057380 RCV000156060 RCV000457442
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Glu82Lys
CA017794
NM_001282626.2:c.244G>A