Canonical Allele Identifier: PA916013649
Gene: SLC35A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 50364
ClinVar RCV Id: RCV000043515 RCV000498343
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269580.1:p.Val359Ile
CA143742
NM_001282651.2:c.1075G>A