Allele Registry

Canonical Allele Identifier: PA2825809173

Gene: NHS HGNC NCBI

ClinVar RCV:

RCV000117794

RCV002390267

RCV002528221

ClinVar Variation:

129778

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129496.1:p.Leu79Val	CA231333 NM_001136024.4:c.235C>G