Canonical Allele Identifier: PA2825983839
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 451165

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157979.2:p.Met3933Thr
CA1908673
NM_001164507.2:c.11798T>C