Canonical Allele Identifier: PA1139724434
Gene: SLC35C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 965658
ClinVar RCV Id: RCV001240162
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_060859.4:p.Ile125Met
CA380202843
NM_018389.5:c.375C>G