Canonical Allele Identifier: PA2741846668
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 2836522
ClinVar RCV Id: RCV003630656
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258137.2:p.Ala8517Thr
CA348770058
NM_001271208.2:c.25549G>A