Canonical Allele Identifier: PA2825982514
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 242433
ClinVar RCV Id: RCV003475836 RCV003514331
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157979.2:p.Glu2431Lys
CA16616822
NM_001164507.2:c.7291G>A