Allele Registry

Canonical Allele Identifier: PA231332

Gene: NHS HGNC NCBI

ClinVar RCV:

RCV000117787

RCV003621503

ClinVar Variation:

129772

HGVS (amino-acid)	Matching Registered Transcripts
NP_938011.1:p.Val662Met	CA231331 NM_198270.4:c.1984G>A