Allele Registry

Canonical Allele Identifier: PA2826143998

Gene: SLC22A8 HGNC NCBI

ClinVar RCV:

RCV004088531

ClinVar Variation:

2223725

HGVS (amino-acid)	Matching Registered Transcripts
NP_001171661.1:p.His20Gln	CA6060020 NM_001184732.2:c.60T>G CA380990381 NM_001184732.2:c.60T>A