Canonical Allele Identifier: PA2826534145
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 643489
ClinVar RCV Id: RCV000797197

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258137.2:p.Asn1008Asp
CA348821028
NM_001271208.2:c.3022A>G