Canonical Allele Identifier: PA1139683263
Gene: SLC35C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 879139
ClinVar RCV Id: RCV001106357
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138738.1:p.Ser7Ala
CA380202081
NM_001145266.1:c.19T>G