Canonical Allele Identifier: PA2580508723
Gene: NAPRT HGNC NCBI

Linked Data

ClinVar Variation Id: 2466623
ClinVar RCV Id: RCV004260824

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_660202.3:p.Arg503Gln
CA187546814
NM_145201.6:c.1508G>A