Canonical Allele Identifier: PA916004226
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 393007
ClinVar RCV Id: RCV000425742 RCV000550442 RCV002506082 RCV004551506
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258137.2:p.Asp6986His
CA1907121
NM_001271208.2:c.20956G>C