Canonical Allele Identifier: PA110209
Gene: SLC2A1 HGNC NCBI

Linked Data

ClinVar Variation Id: 871442
ClinVar RCV Id: RCV001091410 RCV001862694 RCV003446617
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_006507.2:p.Pro485Leu
CA339952336
NM_006516.4:c.1454C>T