Canonical Allele Identifier: PA2825410775
Gene: SLC35A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 2074716
ClinVar RCV Id: RCV002962982 RCV002962983
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001035963.1:p.Ala344Ser
CA10406072
NM_001042498.3:c.1030G>T