Canonical Allele Identifier: PA2825884466
Gene: SLC35C1 HGNC NCBI

Linked Data

ClinVar Variation Id: 844083
ClinVar RCV Id: RCV001046850
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001138737.1:p.Thr72Met
CA5958210
NM_001145265.2:c.215C>T