Canonical Allele Identifier: PA2580508721
Gene: NAPRT HGNC NCBI

Linked Data

ClinVar Variation Id: 2206973
ClinVar RCV Id: RCV004071372
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_660202.3:p.Glu485Gly
CA4912617
NM_145201.6:c.1454A>G