Canonical Allele Identifier: PA2580179846
Gene: NEB HGNC NCBI
ClinVar RCV:
RCV002575381
ClinVar Variation:
1899263
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258137.2:p.Lys8470Arg
CA348770869
NM_001271208.2:c.25409A>G