Canonical Allele Identifier: PA2825993769
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 1380340
ClinVar RCV Id: RCV001892219

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157980.2:p.Ser8099Cys
CA348778734
NM_001164508.2:c.24295A>T