Canonical Allele Identifier: PA113692
Gene: APRT HGNC NCBI

Linked Data

ClinVar Variation Id: 41012
ClinVar RCV Id: RCV000033909
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000476.1:p.Val150Phe
CA343887
NM_000485.3:c.448G>T