Canonical Allele Identifier: PA2827141959
Gene: ADA HGNC NCBI

Linked Data

ClinVar Variation Id: 863612
ClinVar RCV Id: RCV001070613
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001308979.1:p.Gly217Arg
CA409118416
NM_001322050.2:c.649G>C
CA409118418
NM_001322050.2:c.649G>A