Canonical Allele Identifier: PA2829733902
Gene: SLC17A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1935059
ClinVar RCV Id: RCV002622928
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036566.1:p.Asp450Gly
CA364719925
NM_012434.5:c.1349A>G