Canonical Allele Identifier: PA2826661727
Gene: SLC35A2 HGNC NCBI

Linked Data

ClinVar Variation Id: 392100
ClinVar RCV Id: RCV000427117 RCV002286410
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001269578.1:p.Met1Val