Canonical Allele Identifier: PA2580179548
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 2164372
ClinVar RCV Id: RCV003088001
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258137.2:p.Lys7521Ala
CA2580063941
NM_001271208.2:c.22561_22562delinsGC