Canonical Allele Identifier: PA2825988195
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 289913
ClinVar RCV Id: RCV000326103 RCV001130401 RCV001578688 RCV002522010
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157980.2:p.Ile1071Leu
CA1910972
NM_001164508.2:c.3211A>C