Canonical Allele Identifier: PA2825885685
Gene: SLC17A8 HGNC NCBI

Linked Data

ClinVar Variation Id: 165243
ClinVar RCV Id: RCV000151880
ClinVar Variation Id: 1310207
ClinVar RCV Id: RCV001757275
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138760.1:p.Gly183Arg
CA177989
NM_001145288.2:c.547G>A
CA386216335
NM_001145288.2:c.547G>C