Allele Registry

Canonical Allele Identifier: PA2825809439

Gene: NHS HGNC NCBI

ClinVar RCV:

RCV000117787

RCV003621503

ClinVar Variation:

129772

HGVS (amino-acid)	Matching Registered Transcripts
NP_001129496.1:p.Val506Met	CA231331 NM_001136024.4:c.1516G>A