Allele Registry

Canonical Allele Identifier: PA2826811877

Gene: NHS HGNC NCBI

ClinVar RCV:

RCV000179566

RCV000876610

RCV002317057

ClinVar Variation:

198289

HGVS (amino-acid)	Matching Registered Transcripts
NP_001278796.1:p.Ser1125Leu	CA203353 NM_001291867.2:c.3374C>T