Canonical Allele Identifier: PA658815496
Gene: SLC2A10 HGNC NCBI

Linked Data

ClinVar Variation Id: 520176

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_110404.1:p.Asn227Ser
CA315755988
NM_030777.4:c.680A>G