Canonical Allele Identifier: PA915971968
Gene: NEB HGNC NCBI

Linked Data

ClinVar Variation Id: 198810
ClinVar RCV Id: RCV000245711 RCV000514389 RCV001085642 RCV001578687
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_004534.3:p.Lys180Arg
CA247643
NM_004543.5:c.539A>G