Canonical Allele Identifier: PA2826000286
Gene: SUMF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2666

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158147.1:p.Arg329Trp
CA115671
NM_001164675.2:c.985C>T