Canonical Allele Identifier: PA150817
Gene: ADA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 120307
ClinVar RCV Id: RCV000106388

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269156.1:p.Trp222Ser
CA150816
NM_001282227.2:c.665G>C