Canonical Allele Identifier: PA2741819307
Gene: NOS2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2688228

Amino-acid Alleles

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