Canonical Allele Identifier: PA2827142180
Gene: ADA HGNC NCBI

Linked Data

ClinVar Variation Id: 1678200

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308980.1:p.Asn304Lys
CA9871435
NM_001322051.2:c.912T>A
CA409118668
NM_001322051.2:c.912T>G