Canonical Allele Identifier: PA2580238373
Gene: SLC17A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 2166954
ClinVar RCV Id: RCV003080339

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001369560.1:p.Asp73Gly
CA3890592
NM_001382631.1:c.218A>G