Canonical Allele Identifier: PA2829541408
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_004534.3:p.Arg3285His
CA1908984
NM_004543.5:c.9854G>A