Canonical Allele Identifier: PA323588
Gene: SLC2A10 HGNC NCBI

Linked Data

ClinVar Variation Id: 213711
ClinVar RCV Id: RCV000199050

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_110404.1:p.Phe49Ile
CA323587
NM_030777.4:c.145T>A