Canonical Allele Identifier: PA1139721559
Gene: SLC17A5 HGNC NCBI

Linked Data

ClinVar Variation Id: 863775
ClinVar RCV Id: RCV001070825
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_036566.1:p.Tyr421Asn
CA3890299
NM_012434.5:c.1261T>A