Canonical Allele Identifier: PA319762
Gene: SLC2A10 HGNC NCBI

Linked Data

ClinVar Variation Id: 213750
ClinVar RCV Id: RCV000195424 RCV000644029 RCV002390520
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_110404.1:p.Asp468Asn
CA319761
NM_030777.4:c.1402G>A