Canonical Allele Identifier: PA916026477
Gene: ADA HGNC NCBI

Linked Data

ClinVar Variation Id: 1968

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308979.1:p.Gly81Arg
CA252008
NM_001322050.2:c.241G>A
CA409120439
NM_001322050.2:c.241G>C