Canonical Allele Identifier: PA342656
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 25396
ClinVar RCV Id: RCV000507691
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Ser231Phe
CA342655
NM_003060.4:c.692C>T