Canonical Allele Identifier: PA2829544418
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_004534.3:p.Thr5681Pro
CA1906766
NM_004543.5:c.17041A>C