Canonical Allele Identifier: PA2826731689
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_001273758.1:p.Val516Ala
CA372448509
NM_001286829.2:c.1547T>C