Canonical Allele Identifier: PA2829543383
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 1524251
ClinVar RCV Id: RCV002049098
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004534.3:p.Gln4827Pro
CA348790831
NM_004543.5:c.14480A>C