Allele Registry

Canonical Allele Identifier: PA916020780

Gene: SLC22A5 HGNC NCBI

ClinVar RCV:

RCV000486229

RCV000984307

ClinVar Variation:

418493

HGVS (amino-acid)	Matching Registered Transcripts
NP_001295051.1:p.Pro305Leu	CA16618116 NM_001308122.2:c.914C>T