Canonical Allele Identifier: PA645457897
Gene: HPRT1 HGNC NCBI

Linked Data

ClinVar Variation Id: 280785
ClinVar RCV Id: RCV000330466
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000185.1:p.Leu68Phe
CA10603704
NM_000194.3:c.202C>T