Canonical Allele Identifier: PA320064
Gene: SLC2A10 HGNC NCBI

Linked Data

ClinVar Variation Id: 213714
ClinVar RCV Id: RCV000195701

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_110404.1:p.Lys196Met
CA320063
NM_030777.4:c.587A>T