Canonical Allele Identifier: PA915972495
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 257815
ClinVar RCV Id: RCV000251605 RCV000514932 RCV001081407
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004534.3:p.Gly1489Asp
CA1910625
NM_004543.5:c.4466G>A