Canonical Allele Identifier: PA2825982110
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 331500

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157979.2:p.Glu1990Lys
CA1910233
NM_001164507.2:c.5968G>A