Allele Registry

Canonical Allele Identifier: PA108429

Gene: SLC22A5 HGNC NCBI

ClinVar RCV:

RCV000526996

RCV001566993

RCV003900147

ClinVar Variation:

460416

HGVS (amino-acid)	Matching Registered Transcripts
NP_003051.1:p.Thr264Arg	CA3403970 NM_003060.4:c.791C>G