Canonical Allele Identifier: PA916012766
Gene: ADA2 HGNC NCBI

Linked Data

ClinVar Variation Id: 420337
ClinVar RCV Id: RCV000484766 RCV001067680 RCV003419802
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269155.1:p.Gly358Arg
CA10087985
NM_001282226.2:c.1072G>A
CA410233181
NM_001282226.2:c.1072G>C