Canonical Allele Identifier: PA2825993249
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 1929162
ClinVar RCV Id: RCV002618593

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157980.2:p.Met7483Leu
CA348764677
NM_001164508.2:c.22447A>T
CA348764682
NM_001164508.2:c.22447A>C