Canonical Allele Identifier: PA2825981021
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 516250

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157979.2:p.Asp847Gly
CA1911190
NM_001164507.2:c.2540A>G