Canonical Allele Identifier: PA263934
Gene: SLC17A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 56560
ClinVar RCV Id: RCV000049973
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036566.1:p.Gly328Glu
CA263933
NM_012434.5:c.983G>A