Allele Registry

Canonical Allele Identifier: PA2826811700

Gene: NHS HGNC NCBI

ClinVar RCV:

RCV000153563

RCV000764867

RCV001349017

RCV002316969

ClinVar Variation:

167351

HGVS (amino-acid)	Matching Registered Transcripts
NP_001278796.1:p.Ala51Val	CA234375 NM_001291867.2:c.152C>T