Canonical Allele Identifier: PA104732
Gene: SLCO2A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 30187
ClinVar RCV Id: RCV000023105
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005621.2:p.Gly255Glu
CA129009
NM_005630.3:c.764G>A