Canonical Allele Identifier: PA1139672601
Gene: APRT HGNC NCBI

Linked Data

ClinVar Variation Id: 988057
ClinVar RCV Id: RCV001269449
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001025189.1:p.Gly120Val
CA397087872
NM_001030018.2:c.359G>T