Allele Registry

Canonical Allele Identifier: PA106903

Gene: PRPS1 HGNC NCBI

ClinVar RCV:

RCV000010610

ClinVar Variation:

9932

HGVS (amino-acid)	Matching Registered Transcripts
NP_002755.1:p.Ala190Val	CA254941 NM_002764.4:c.569C>T