Allele Registry

Canonical Allele Identifier: PA916020818

Gene: SLC22A5 HGNC NCBI

ClinVar RCV:

RCV000022365

RCV000224074

ClinVar Variation:

25411

HGVS (amino-acid)	Matching Registered Transcripts
NP_001295051.1:p.Pro422Leu	CA342672 NM_001308122.2:c.1265C>T