Canonical Allele Identifier: PA2825993229
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 2038599
ClinVar RCV Id: RCV002895076 RCV004065987
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157980.2:p.Arg7466His
CA1906658
NM_001164508.2:c.22397G>A