Canonical Allele Identifier: PA2827142071
Gene: ADA HGNC NCBI

Linked Data

ClinVar Variation Id: 960745
ClinVar RCV Id: RCV001234325

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308980.1:p.Ser191Asn
CA409120803
NM_001322051.2:c.572G>A