Canonical Allele Identifier: PA645425026
Gene: SLC17A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 431079
ClinVar RCV Id: RCV000496107 RCV001332964 RCV001548541
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036566.1:p.Arg39His
CA3890602
NM_012434.5:c.116G>A