Canonical Allele Identifier: PA2826659563
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 1442001
ClinVar RCV Id: RCV001968068
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Gln30Glu
CA342807364
NM_001282626.2:c.88C>G