Canonical Allele Identifier: PA2826731684
Gene: NAPRT HGNC NCBI

Linked Data

ClinVar Variation Id: 2206973
ClinVar RCV Id: RCV004071372
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001273758.1:p.Glu472Gly
CA4912617
NM_001286829.2:c.1415A>G