Canonical Allele Identifier: PA2825005063
Gene: ADA HGNC NCBI

Linked Data

ClinVar Variation Id: 2046831
ClinVar RCV Id: RCV002913911

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000013.2:p.Phe7Leu
CA409122592
NM_000022.3:c.21C>A
CA409122593
NM_000022.3:c.21C>G
CA409122599
NM_000022.3:c.19T>C