Canonical Allele Identifier: PA1139765638
Gene: SLC2A10 HGNC NCBI

Linked Data

ClinVar Variation Id: 898986
ClinVar RCV Id: RCV001143186 RCV001586003 RCV002355124
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_110404.1:p.Pro211Leu
CA9892013
NM_030777.4:c.632C>T