Canonical Allele Identifier: PA108371
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 379259
ClinVar RCV Id: RCV000439652 RCV001237032
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Ser26Asn
CA3403778
NM_003060.4:c.77G>A