Canonical Allele Identifier: PA2826000282
Gene: SUMF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2676
ClinVar RCV Id: RCV000002795

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158147.1:p.Ala328Pro
CA115679
NM_001164675.2:c.982G>C