Allele Registry

Canonical Allele Identifier: PA105189

Gene: HPRT1 HGNC NCBI

ClinVar Allele:

25086

ClinVar RCV:

RCV000010747

RCV001250108

ClinVar Variation:

10047

HGVS (amino-acid)	Matching Registered Transcripts
NP_000185.1:p.His204Asp	CA254999 NM_000194.3:c.610C>G