Canonical Allele Identifier: PA113948
Gene: OAT HGNC NCBI

Linked Data

ClinVar Variation Id: 158
ClinVar RCV Id: RCV000000181
ClinVar Variation Id: 56116
ClinVar RCV Id: RCV000049525 RCV000513174
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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