Canonical Allele Identifier: PA658667278
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 460395
ClinVar RCV Id: RCV000555770 RCV000602546 RCV001696988
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Met417Val
CA3404104
NM_003060.4:c.1249A>G