Allele Registry

Canonical Allele Identifier: PA916018186

Gene: NHS HGNC NCBI

ClinVar RCV:

RCV000190792

RCV000594957

RCV002514089

ClinVar Variation:

208770

HGVS (amino-acid)	Matching Registered Transcripts
NP_001278796.1:p.Arg392Gln	CA204863 NM_001291867.2:c.1175G>A