Allele Registry

Canonical Allele Identifier: PA2826144098

Gene: SLC22A8 HGNC NCBI

ClinVar RCV:

RCV001620273

ClinVar Variation:

1232453

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171665.1:p.Ile182Phe	CA6059770 NM_001184736.2:c.544A>T