Canonical Allele Identifier: PA2741846063
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 2850528
ClinVar RCV Id: RCV003630877
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258137.2:p.Ser5947Asn
CA1908095
NM_001271208.2:c.17840G>A