Canonical Allele Identifier: PA2825884652
Gene: SLC35C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 530694
ClinVar RCV Id: RCV000636675
ClinVar Variation Id: 936186
ClinVar RCV Id: RCV001204930
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138738.1:p.Gln27His
CA380202300
NM_001145266.1:c.81G>C
CA380202302
NM_001145266.1:c.81G>T