Canonical Allele Identifier: PA2825992339
Gene: NEB HGNC NCBI
ClinVar RCV:
RCV002750571
ClinVar Variation:
1973518
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157980.2:p.Arg6477Ser
CA348791913
NM_001164508.2:c.19429C>A