Canonical Allele Identifier: PA2825991745
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 331465
ClinVar RCV Id: RCV000795724 RCV002487462 RCV003129840
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157980.2:p.Arg5821His
CA1908205
NM_001164508.2:c.17462G>A