Canonical Allele Identifier: PA2573196767
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 1380340
ClinVar RCV Id: RCV001892219
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258137.2:p.Ser8134Cys
CA348778734
NM_001271208.2:c.24400A>T