Allele Registry

Canonical Allele Identifier: PA204864

Gene: NHS HGNC NCBI

ClinVar Allele:

205337

ClinVar RCV:

RCV000190792

RCV000594957

RCV002514089

ClinVar Variation:

208770

HGVS (amino-acid)	Matching Registered Transcripts
NP_938011.1:p.Arg371Gln	CA204863 NM_198270.4:c.1112G>A