Canonical Allele Identifier: PA915972316
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 289913
ClinVar RCV Id: RCV000326103 RCV001130401 RCV001578688 RCV002522010
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004534.3:p.Ile1071Leu
CA1910972
NM_004543.5:c.3211A>C