Canonical Allele Identifier: PA2825410766
Gene: SLC35A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 932491
ClinVar RCV Id: RCV001200322 RCV003741248
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035963.1:p.Ala328Thr
CA10406077
NM_001042498.3:c.982G>A