Allele Registry

Canonical Allele Identifier: PA916018228

Gene: NHS HGNC NCBI

ClinVar RCV:

RCV000498961

ClinVar Variation:

375706

HGVS (amino-acid)	Matching Registered Transcripts
NP_001278796.1:p.Ser1483Cys	CA412370422 NM_001291867.2:c.4448C>G