Canonical Allele Identifier: PA2825987168
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 194453
ClinVar RCV Id: RCV000202808 RCV000415163 RCV000724204 RCV001080816 RCV004552967
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157979.2:p.Thr8456Met
CA240416
NM_001164507.2:c.25367C>T