Canonical Allele Identifier: PA2825999779
Gene: SUMF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 371554
ClinVar RCV Id: RCV000412333

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158146.1:p.Gly222Arg
CA16040928
NM_001164674.2:c.664G>C