Canonical Allele Identifier: PA645425097
Gene: SLC17A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 235209
ClinVar RCV Id: RCV000224654 RCV000327513 RCV001164158 RCV001083032 RCV004532820
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036566.1:p.Val442Ile
CA3890290
NM_012434.5:c.1324G>A