Canonical Allele Identifier: PA110084
Gene: SLC2A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2202742
ClinVar RCV Id: RCV002634288

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006507.2:p.Asn317Thr
CA339956442
NM_006516.4:c.950A>C