Canonical Allele Identifier: PA2825999752
Gene: SUMF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2677
ClinVar RCV Id: RCV000002796
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158146.1:p.Cys193Tyr
CA115680
NM_001164674.2:c.578G>A