Allele Registry

Canonical Allele Identifier: PA104692

Gene: SLC2A9 HGNC NCBI

ClinVar RCV:

RCV000201283

ClinVar Variation:

217421

HGVS (amino-acid)	Matching Registered Transcripts
NP_064425.2:p.Thr125Met	CA210117 NM_020041.3:c.374C>T