Canonical Allele Identifier: PA2828079822
Gene: NAPRT HGNC NCBI

Linked Data

ClinVar Variation Id: 3175306
ClinVar RCV Id: RCV004466635

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350075.1:p.Leu271Gln
CA4912606
NM_001363146.1:c.812T>A