Canonical Allele Identifier: PA2825986201
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 506284
ClinVar RCV Id: RCV000611555
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157979.2:p.Thr7382Pro
CA1906766
NM_001164507.2:c.22144A>C