Canonical Allele Identifier: PA2825884437
Gene: SLC35C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1421297
ClinVar RCV Id: RCV001916852
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138737.1:p.Asn16His
CA380202172
NM_001145265.2:c.46A>C