Canonical Allele Identifier: PA2829544535
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 129731
ClinVar RCV Id: RCV000117746 RCV000665740
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004534.3:p.Arg5777Cys
CA231313
NM_004543.5:c.17329C>T