Canonical Allele Identifier: PA2825980716
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 290878
ClinVar RCV Id: RCV000355760 RCV000691778 RCV002504024
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157979.2:p.Asn517Ser
CA1911541
NM_001164507.2:c.1550A>G