Canonical Allele Identifier: PA2826000162
Gene: SUMF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2677
ClinVar RCV Id: RCV000002796

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158147.1:p.Cys218Tyr
CA115680
NM_001164675.2:c.653G>A