Canonical Allele Identifier: PA1139724356
Gene: SLC35C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 846744
ClinVar RCV Id: RCV001050132
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060859.4:p.Lys7Glu
CA5958167
NM_018389.5:c.19A>G