Canonical Allele Identifier: PA891848710
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 581634
ClinVar RCV Id: RCV000705521 RCV002226490
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Ser231Cys
CA360805014
NM_003060.4:c.692C>G