Canonical Allele Identifier: PA2825986280
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 1905936
ClinVar RCV Id: RCV002583881 RCV003134450
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157979.2:p.His7471Tyr
CA348764826
NM_001164507.2:c.22411C>T