Canonical Allele Identifier: PA1139750271
Gene: SUMF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 989687
ClinVar RCV Id: RCV001277570
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_877437.2:p.Val209Ala
CA2230515
NM_182760.4:c.626T>C