Canonical Allele Identifier: PA658676006
Gene: SLC17A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 452551
ClinVar RCV Id: RCV000522096 RCV001114670
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_647480.1:p.Thr57Met
CA6738683
NM_139319.3:c.170C>T