Canonical Allele Identifier: PA174678
Gene: SLC2A4RG HGNC NCBI

Linked Data

ClinVar Variation Id: 161728
ClinVar RCV Id: RCV000149264
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_064446.2:p.Arg354Ser
CA174677
NM_020062.4:c.1060C>A