Canonical Allele Identifier: PA2828079802
Gene: NAPRT HGNC NCBI

Linked Data

ClinVar Variation Id: 2354303
ClinVar RCV Id: RCV004192778

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001350074.1:p.Leu472Met
CA187546895
NM_001363145.1:c.1414C>A