ClinGen Allele Registry
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Canonical Allele Identifier:
PA113948
Gene: OAT
HGNC
NCBI
Linked Data - NCBI & NCI
ClinVar Allele:
15197
70755
ClinVar RCV:
RCV000000181
RCV000049525
RCV000513174
ClinVar Variation:
158
56116
JSON-LD
Amino-acid Alleles
HGVS (amino-acid)
Matching Registered Transcripts
NP_001165285.1:p.Leu299Phe
CA113946
NM_001171814.2:c.897G>C
CA144141
NM_001171814.2:c.897G>T