Canonical Allele Identifier: PA252018
Gene: ADA HGNC NCBI
ClinVar Allele:
ClinVar RCV:
ClinVar Variation:

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000013.2:p.Gly74Val
CA252016
NM_000022.3:c.221G>T