Canonical Allele Identifier: PA2825981540
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 2077546
ClinVar RCV Id: RCV002976555
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157979.2:p.Ala1396Val
CA1910702
NM_001164507.2:c.4187C>T