Canonical Allele Identifier: PA174113
Gene: ST8SIA6 HGNC NCBI

Linked Data

ClinVar Variation Id: 161480
ClinVar RCV Id: RCV000149014
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001004470.1:p.Trp115Leu
CA174112
NM_001004470.3:c.344G>T