Allele Registry

Canonical Allele Identifier: PA1139695452

Gene: SLC22A5 HGNC NCBI

ClinVar RCV:

RCV001216413

ClinVar Variation:

945707

HGVS (amino-acid)	Matching Registered Transcripts
NP_001295051.1:p.Arg193Pro	CA360804515 NM_001308122.2:c.578G>C