Allele Registry

Canonical Allele Identifier: PA2826924032

Gene: SLC22A5 HGNC NCBI

ClinVar RCV:

RCV000022298

RCV000730713

RCV000731644

RCV001386840

ClinVar Variation:

25351

595954

HGVS (amino-acid)	Matching Registered Transcripts
NP_001295051.1:p.Arg19Pro	CA342608 NM_001308122.2:c.56G>C CA913190144 NM_001308122.2:c.56_57delinsCT