Canonical Allele Identifier: PA2580133586
Gene: APRT HGNC NCBI

Linked Data

ClinVar Variation Id: 2115627
ClinVar RCV Id: RCV003046556
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001025189.1:p.Val126del
CA2580613920
NM_001030018.2:c.375_377del