Canonical Allele Identifier: PA2826731688
Gene: NAPRT HGNC NCBI

Linked Data

ClinVar Variation Id: 2372797
ClinVar RCV Id: RCV004214740

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273758.1:p.Arg497Gln
CA4912600
NM_001286829.2:c.1490G>A