Canonical Allele Identifier: PA174849
Gene: SLC35G1 HGNC NCBI

Linked Data

ClinVar Variation Id: 161821
ClinVar RCV Id: RCV000149357
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_694958.1:p.Ala142Thr
CA174848
NM_153226.4:c.424G>A