Canonical Allele Identifier: PA2828909618
Gene: SLC17A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 2306464
ClinVar RCV Id: RCV002869898

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369559.1:p.Thr178Ala
CA140973834
NM_001382630.1:c.532A>G