Canonical Allele Identifier: PA2580179273
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 1973518
ClinVar RCV Id: RCV002750571
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001258137.2:p.Arg6477Ser
CA348791913
NM_001271208.2:c.19429C>A