Allele Registry

Canonical Allele Identifier: PA2741819307

Gene: NOS2 HGNC NCBI

ClinVar RCV:

RCV003489137

RCV003980962

ClinVar Variation:

2688228

HGVS (amino-acid)	Matching Registered Transcripts
NP_000616.3:p.Ser608Leu	CA8454610 NM_000625.4:c.1823C>T