Allele Registry

Canonical Allele Identifier: PA108097

Gene: SLC22A5 HGNC NCBI

ClinVar RCV:

RCV000006791

ClinVar Variation:

6422

HGVS (amino-acid)	Matching Registered Transcripts
NP_003051.1:p.Arg169Trp	CA340585 NM_003060.4:c.505C>T