Canonical Allele Identifier: PA658667182
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 460405
ClinVar RCV Id: RCV000530205 RCV002226470 RCV001556640
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Asn91Ser
CA3403831
NM_003060.4:c.272A>G