Canonical Allele Identifier: PA2826657558
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 2773538
ClinVar RCV Id: RCV003532555
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Gln170Lys
CA342817319
NM_001282624.2:c.508C>A