Canonical Allele Identifier: PA318476
Gene: SLC2A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 207215
ClinVar Variation Id: 207216

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006507.2:p.Gly470Arg
CA318475
NM_006516.4:c.1408G>A
CA318477
NM_006516.4:c.1408G>C