Canonical Allele Identifier: PA2829542490
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 331465
ClinVar RCV Id: RCV000795724 RCV002487462 RCV003129840
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004534.3:p.Arg4120His
CA1908205
NM_004543.5:c.12359G>A