Allele Registry

Canonical Allele Identifier: PA645502266

Gene: SLC22A5 HGNC NCBI

ClinVar RCV:

RCV000481536

RCV001067038

ClinVar Variation:

418492

HGVS (amino-acid)	Matching Registered Transcripts
NP_003051.1:p.Pro68Ser	CA16618115 NM_003060.4:c.202C>T