ClinGen Allele Registry
Allele Registry
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Canonical Allele Identifier:
PA113692
Gene: APRT
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
49434
ClinVar RCV:
RCV000033909
ClinVar Variation:
41012
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_000476.1:p.Val150Phe
CA343887
NM_000485.3:c.448G>T