Canonical Allele Identifier: PA2829544522
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 1380772
ClinVar RCV Id: RCV001917309 RCV003130573
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004534.3:p.Gly5771Ser
CA1906653
NM_004543.5:c.17311G>A