Canonical Allele Identifier: PA916003279
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 331480
ClinVar RCV Id: RCV000822266 RCV001753794 RCV002480174
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258137.2:p.Arg3528His
CA1908984
NM_001271208.2:c.10583G>A