Canonical Allele Identifier: PA2828079826
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_001350075.1:p.Val301Ala
CA372448509
NM_001363146.1:c.902T>C