Canonical Allele Identifier: PA2825992384
Gene: NEB HGNC NCBI
ClinVar RCV:
RCV002049098
ClinVar Variation:
1524251
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157980.2:p.Gln6528Pro
CA348790831
NM_001164508.2:c.19583A>C