Canonical Allele Identifier: PA2826662267
Gene: SLC35A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 754204
ClinVar RCV Id: RCV001523443
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269580.1:p.Ala383Thr
CA10406065
NM_001282651.2:c.1147G>A