Canonical Allele Identifier: PA2825993155
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 506284
ClinVar RCV Id: RCV000611555

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157980.2:p.Thr7382Pro
CA1906766
NM_001164508.2:c.22144A>C