Canonical Allele Identifier: PA105190
Gene: SLC35A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 135676
ClinVar RCV Id: RCV000122746
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_005651.1:p.Ser213Phe
CA163127
NM_005660.3:c.638C>T