Canonical Allele Identifier: PA2825983816
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 129707
ClinVar RCV Id: RCV000117722 RCV000549434
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157979.2:p.Asp3910Gly
CA153884
NM_001164507.2:c.11729A>G