Canonical Allele Identifier: PA2825999735
Gene: SUMF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 1496993
ClinVar RCV Id: RCV002019318

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158146.1:p.Pro177Gln
CA2230522
NM_001164674.2:c.530C>A