Canonical Allele Identifier: PA2829543796
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_004534.3:p.Ala5184Val
CA1907204
NM_004543.5:c.15551C>T