Canonical Allele Identifier: PA2826661835
Gene: SLC35A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 224808
ClinVar RCV Id: RCV000210405
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269578.1:p.Tyr206Cys
CA357924
NM_001282649.2:c.617A>G