Canonical Allele Identifier: PA2829545477
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_004534.3:p.Thr6600Met
CA240416
NM_004543.5:c.19799C>T