Allele Registry

Canonical Allele Identifier: PA2580288786

Gene: SLC22A8 HGNC NCBI

ClinVar RCV:

RCV004088531

ClinVar Variation:

2223725

HGVS (amino-acid)	Matching Registered Transcripts
NP_004245.2:p.His20Gln	CA6060020 NM_004254.4:c.60T>G CA380990381 NM_004254.4:c.60T>A