Canonical Allele Identifier: PA2825990778
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 129707
ClinVar RCV Id: RCV000117722 RCV000549434
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157980.2:p.Asp3910Gly
CA153884
NM_001164508.2:c.11729A>G