Canonical Allele Identifier: PA2825986291
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_001157979.2:p.Arg7478Cys
CA231313
NM_001164507.2:c.22432C>T