Canonical Allele Identifier: PA2580508722
Gene: NAPRT HGNC NCBI

Linked Data

ClinVar Variation Id: 2354303
ClinVar RCV Id: RCV004192778

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_660202.3:p.Leu499Met
CA187546895
NM_145201.6:c.1495C>A