Allele Registry

Canonical Allele Identifier: PA658807670

Gene: SLC22A5 HGNC NCBI

ClinVar Variation Id: 529850

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