Canonical Allele Identifier: PA129398
Gene: SUMF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 30689
ClinVar RCV Id: RCV000023667
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_877437.2:p.Gly263Val
CA129397
NM_182760.4:c.788G>T