Canonical Allele Identifier: PA2825982520
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 533993
ClinVar RCV Id: RCV000641337 RCV001662690 RCV002507092
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001157979.2:p.Arg2437Trp
CA1909881
NM_001164507.2:c.7309C>T