Canonical Allele Identifier: PA2830270161
Gene: NAPRT HGNC NCBI

Linked Data

ClinVar Variation Id: 3175314
ClinVar RCV Id: RCV004466643
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_660202.3:p.Val529Ala
CA372448509
NM_145201.6:c.1586T>C