Canonical Allele Identifier: PA2825992369
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 199250
ClinVar RCV Id: RCV000180772 RCV000700979
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157980.2:p.Arg6515His
CA248354
NM_001164508.2:c.19544G>A