Allele Registry

Canonical Allele Identifier: PA105332

Gene: HPRT1 HGNC NCBI

ClinVar Allele:

25101

ClinVar RCV:

RCV000010765

ClinVar Variation:

10062

HGVS (amino-acid)	Matching Registered Transcripts
NP_000185.1:p.Met143Lys	CA255004 NM_000194.3:c.428T>A