Allele Registry

Canonical Allele Identifier: PA246848

Gene: NHS HGNC NCBI

ClinVar Allele:

195452

ClinVar RCV:

RCV000179568

RCV002444719

RCV003509508

ClinVar Variation:

198291

HGVS (amino-acid)	Matching Registered Transcripts
NP_938011.1:p.Gly422Arg	CA246847 NM_198270.4:c.1264G>A CA412350911 NM_198270.4:c.1264G>C