Canonical Allele Identifier: PA2825992710
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 281478
ClinVar RCV Id: RCV000292919 RCV000535305 RCV002502095 RCV002518819
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157980.2:p.Ala6885Val
CA1907204
NM_001164508.2:c.20654C>T