Canonical Allele Identifier: PA916013584
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 499648
ClinVar RCV Id: RCV000594221
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269553.1:p.Leu84Val
CA342815647
NM_001282624.2:c.250C>G