Allele Registry

Canonical Allele Identifier: PA916020835

Gene: SLC22A5 HGNC NCBI

ClinVar RCV:

RCV001924022

ClinVar Variation:

1424767

HGVS (amino-acid)	Matching Registered Transcripts
NP_001295051.1:p.Val470Phe	CA342676 NM_001308122.2:c.1408G>T