Canonical Allele Identifier: PA2826000144
Gene: SUMF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1496993
ClinVar RCV Id: RCV002019318
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158147.1:p.Pro202Gln
CA2230522
NM_001164675.2:c.605C>A