Canonical Allele Identifier: PA177990
Gene: SLC17A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 165243
ClinVar RCV Id: RCV000151880
ClinVar Variation Id: 1310207
ClinVar RCV Id: RCV001757275
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_647480.1:p.Gly183Arg
CA177989
NM_139319.3:c.547G>A
CA386216335
NM_139319.3:c.547G>C