Canonical Allele Identifier: PA2829545449
Gene: NEB HGNC NCBI
ClinVar RCV:
RCV002575381
ClinVar Variation:
1899263
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004534.3:p.Lys6579Arg
CA348770869
NM_004543.5:c.19736A>G