Canonical Allele Identifier: PA2828079821
Gene: NAPRT HGNC NCBI

Linked Data

ClinVar Variation Id: 2206973
ClinVar RCV Id: RCV004071372
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350075.1:p.Glu257Gly
CA4912617
NM_001363146.1:c.770A>G