Canonical Allele Identifier: PA2826000169
Gene: SUMF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 3172095
ClinVar RCV Id: RCV004461037

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158147.1:p.Arg224Pro
CA351632599
NM_001164675.2:c.671G>C