Allele Registry

Canonical Allele Identifier: PA916018189

Gene: NHS HGNC NCBI

ClinVar RCV:

RCV000179568

RCV002444719

RCV003509508

ClinVar Variation:

198291

HGVS (amino-acid)	Matching Registered Transcripts
NP_001278796.1:p.Gly443Arg	CA246847 NM_001291867.2:c.1327G>A CA412350911 NM_001291867.2:c.1327G>C