Canonical Allele Identifier: PA325129
Gene: SLC2A10 HGNC NCBI

Linked Data

ClinVar Variation Id: 213722
ClinVar RCV Id: RCV000200540 RCV000700242 RCV002408873
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_110404.1:p.Leu353Val
CA325128
NM_030777.4:c.1057C>G