Canonical Allele Identifier: PA658807670
Gene: SLC22A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 529850
ClinVar RCV Id: RCV000635350 RCV001785686 RCV002226475
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_003051.1:p.Thr337Ile
CA3404040
NM_003060.4:c.1010C>T