Canonical Allele Identifier: PA916004648
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 331407
ClinVar RCV Id: RCV000641466 RCV003129837
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258137.2:p.Ile8288Val
CA1905932
NM_001271208.2:c.24862A>G