Canonical Allele Identifier: PA915972729
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 331500
ClinVar RCV Id: RCV000712395 RCV001082132
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004534.3:p.Glu1990Lys
CA1910233
NM_004543.5:c.5968G>A