Canonical Allele Identifier: PA319967
Gene: SLC2A10 HGNC NCBI

Linked Data

ClinVar Variation Id: 161106
ClinVar RCV Id: RCV000195605 RCV000202453 RCV004019778
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_110404.1:p.Arg231Trp
CA319966
NM_030777.4:c.691C>T