Canonical Allele Identifier: PA2825994100
Gene: NEB HGNC NCBI
ClinVar RCV:
RCV002575381
ClinVar Variation:
1899263
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157980.2:p.Lys8435Arg
CA348770869
NM_001164508.2:c.25304A>G