Canonical Allele Identifier: PA2828079805
Gene: NAPRT HGNC NCBI

Linked Data

ClinVar Variation Id: 3175314
ClinVar RCV Id: RCV004466643
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350074.1:p.Val502Ala
CA372448509
NM_001363145.1:c.1505T>C