Canonical Allele Identifier: PA2825999873
Gene: SUMF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2668
ClinVar RCV Id: RCV000002787
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158146.1:p.Cys311Arg
CA115673
NM_001164674.2:c.931T>C