Canonical Allele Identifier: PA104716
Gene: SLCO2A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 438675
ClinVar RCV Id: RCV000505666 RCV001527659 RCV002527331
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005621.2:p.Gly222Arg
CA2626753
NM_005630.3:c.664G>A
CA354617930
NM_005630.3:c.664G>C