Canonical Allele Identifier: PA110056
Gene: SLC2A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 16120
ClinVar RCV Id: RCV000017500 RCV001548577 RCV002271988
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006507.2:p.Arg468Trp
CA019072
NM_006516.4:c.1402C>T