Canonical Allele Identifier: PA2573196343
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 1524251
ClinVar RCV Id: RCV002049098
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258137.2:p.Gln6528Pro
CA348790831
NM_001271208.2:c.19583A>C