Canonical Allele Identifier: PA2825999885
Gene: SUMF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2676
ClinVar RCV Id: RCV000002795

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158146.1:p.Ala323Pro
CA115679
NM_001164674.2:c.967G>C