Canonical Allele Identifier: PA2826000101
Gene: SUMF1 HGNC NCBI

Linked Data

ClinVar Variation Id: 2672

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001158147.1:p.Ser155Pro
CA115675
NM_001164675.2:c.463T>C