Canonical Allele Identifier: PA2826659645
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 424915
ClinVar RCV Id: RCV000488077 RCV000816556
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Glu53Gly
CA16621576
NM_001282626.2:c.158A>G