Canonical Allele Identifier: PA2830270157
Gene: NAPRT HGNC NCBI

Linked Data

ClinVar Variation Id: 3175295
ClinVar RCV Id: RCV004466624
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_660202.3:p.Glu410Lys
CA4912724
NM_145201.6:c.1228G>A