Canonical Allele Identifier: PA103969
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_000265.1:p.Leu437Phe
CA113946
NM_000274.4:c.1311G>C
CA144141
NM_000274.4:c.1311G>T