Canonical Allele Identifier: PA2826611528
Gene: SLC2A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 16095
ClinVar RCV Id: RCV000017475

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001265587.1:p.Pro298Leu
CA019992
NM_001278658.2:c.893C>T