Canonical Allele Identifier: PA2825989476
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 242433

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157980.2:p.Glu2431Lys
CA16616822
NM_001164508.2:c.7291G>A