Allele Registry

Canonical Allele Identifier: PA2829418975

Gene: SLC22A5 HGNC NCBI

ClinVar Variation Id: 1951950

HGVS (amino-acid)	Matching Registered Transcripts
NP_003051.1:p.Phe189Leu	CA127208797 NM_003060.4:c.565T>C CA360804745 NM_003060.4:c.567C>A CA360804746 NM_003060.4:c.567C>G