Allele Registry

Canonical Allele Identifier: PA2826812001

Gene: NHS HGNC NCBI

ClinVar RCV:

RCV000179569

RCV001520145

RCV002399640

ClinVar Variation:

198292

HGVS (amino-acid)	Matching Registered Transcripts
NP_001278797.1:p.Val337Met	CA246849 NM_001291868.2:c.1009G>A