Canonical Allele Identifier: PA913200244
Gene: SLC2A10 HGNC NCBI

Linked Data

ClinVar Variation Id: 626893
ClinVar RCV Id: RCV000770705

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_110404.1:p.Asp197Gly
CA409267330
NM_030777.4:c.590A>G