Allele Registry

Canonical Allele Identifier: PA106492

Gene: SUMF1 HGNC NCBI

ClinVar Allele:

17714

ClinVar RCV:

RCV000002794

ClinVar Variation:

2675

HGVS (amino-acid)	Matching Registered Transcripts
NP_877437.2:p.Arg345Cys	CA115678 NM_182760.4:c.1033C>T