Allele Registry

Canonical Allele Identifier: PA916018192

Gene: NHS HGNC NCBI

ClinVar RCV:

RCV000179569

RCV001520145

RCV002399640

ClinVar Variation:

198292

HGVS (amino-acid)	Matching Registered Transcripts
NP_001278796.1:p.Val535Met	CA246849 NM_001291867.2:c.1603G>A