Canonical Allele Identifier: PA916004158
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 281478
ClinVar RCV Id: RCV000292919 RCV000535305 RCV002502095 RCV002518819
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258137.2:p.Ala6885Val
CA1907204
NM_001271208.2:c.20654C>T