Allele Registry

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Canonical Allele Identifier: PA2825884442

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_001138737.1:p.Gln27His	CA380202300 NM_001145265.2:c.81G>C CA380202302 NM_001145265.2:c.81G>T