Canonical Allele Identifier: PA2825937347
Gene: NOS3 HGNC NCBI

Linked Data

ClinVar Variation Id: 2323587
ClinVar RCV Id: RCV004164982

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001153582.1:p.Ala520Val
CA369858256
NM_001160110.1:c.1559C>T