Canonical Allele Identifier: PA302823
Gene: SLC2A10 HGNC NCBI

Linked Data

ClinVar Variation Id: 139172

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_110404.1:p.Ala206Thr
CA302822
NM_030777.4:c.616G>A