Canonical Allele Identifier: PA2825994141
Gene: NEB HGNC NCBI
ClinVar RCV:
RCV003630656
ClinVar Variation:
2836522
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157980.2:p.Ala8482Thr
CA348770058
NM_001164508.2:c.25444G>A