Allele Registry

Canonical Allele Identifier: PA231334

Gene: NHS HGNC NCBI

ClinVar RCV:

RCV000117794

RCV002390267

RCV002528221

ClinVar Variation:

129778

HGVS (amino-acid)	Matching Registered Transcripts
NP_938011.1:p.Leu256Val	CA231333 NM_198270.4:c.766C>G