Allele Registry

Canonical Allele Identifier: PA645493473

Gene: NHS HGNC NCBI

ClinVar RCV:

RCV000498961

ClinVar Variation:

375706

HGVS (amino-acid)	Matching Registered Transcripts
NP_938011.1:p.Ser1462Cys	CA412370422 NM_198270.4:c.4385C>G