Allele Registry

Canonical Allele Identifier: PA2826144011

Gene: SLC22A8 HGNC NCBI

ClinVar RCV:

RCV001620273

ClinVar Variation:

1232453

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171661.1:p.Ile305Phe	CA6059770 NM_001184732.2:c.913A>T