Canonical Allele Identifier: PA645469271
Gene: SLC2A10 HGNC NCBI

Linked Data

ClinVar Variation Id: 418496
ClinVar RCV Id: RCV000486994

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_110404.1:p.Leu238Val
CA9892031
NM_030777.4:c.712C>G