Canonical Allele Identifier: PA2828911069
Gene: SLC17A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1492082
ClinVar RCV Id: RCV002010231 RCV002608063
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369565.1:p.Val333Ala
CA3890293
NM_001382636.1:c.998T>C