Canonical Allele Identifier: PA2573199540
Gene: ADA HGNC NCBI

Linked Data

ClinVar Variation Id: 1523684
ClinVar RCV Id: RCV002039064

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308980.1:p.Glu13Lys
CA409122544
NM_001322051.2:c.37G>A
CA2573157145
NM_001322051.2:c.36_37delinsAA