Allele Registry

Canonical Allele Identifier: PA658667209

Gene: SLC22A5 HGNC NCBI

ClinVar RCV:

RCV000556789

ClinVar Variation:

460412

HGVS (amino-acid)	Matching Registered Transcripts
NP_003051.1:p.Phe230Leu	CA127209308 NM_003060.4:c.688T>C CA360805009 NM_003060.4:c.690C>A CA360805010 NM_003060.4:c.690C>G