Canonical Allele Identifier: PA2825884499
Gene: SLC35C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1476369
ClinVar RCV Id: RCV001977917

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138737.1:p.Tyr124Ser
CA380202921
NM_001145265.2:c.371A>C