Allele Registry

Canonical Allele Identifier: PA916020783

Gene: SLC22A5 HGNC NCBI

ClinVar RCV:

RCV001924005

ClinVar Variation:

1424747

HGVS (amino-acid)	Matching Registered Transcripts
NP_001295051.1:p.Trp307Arg	CA342662 NM_001308122.2:c.919T>C CA343116 NM_001308122.2:c.919T>A