Canonical Allele Identifier: PA2828910637
Gene: SLC17A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 1935059
ClinVar RCV Id: RCV002622928
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369563.1:p.Asp397Gly
CA364719925
NM_001382634.1:c.1190A>G