Allele Registry

Canonical Allele Identifier: PA234376

Gene: NHS HGNC NCBI

ClinVar RCV:

RCV000153563

RCV000764867

RCV001349017

RCV002316969

ClinVar Variation:

167351

HGVS (amino-acid)	Matching Registered Transcripts
NP_938011.1:p.Ala51Val	CA234375 NM_198270.4:c.152C>T