Allele Registry

Canonical Allele Identifier: PA2825809335

Gene: NHS HGNC NCBI

ClinVar RCV:

RCV000179569

RCV001520145

RCV002399640

ClinVar Variation:

198292

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129496.1:p.Val358Met	CA246849 NM_001136024.4:c.1072G>A