Canonical Allele Identifier: PA2825884479
Gene: SLC35C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1356288
ClinVar RCV Id: RCV001876691
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138737.1:p.Asp97Glu
CA380202755
NM_001145265.2:c.291C>A
CA380202756
NM_001145265.2:c.291C>G