Canonical Allele Identifier: PA2826660395
Gene: LMNA HGNC NCBI

Linked Data

ClinVar Variation Id: 500094
ClinVar RCV Id: RCV000593452
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269555.1:p.Leu389Pro
CA342820807
NM_001282626.2:c.1166T>C