Allele Registry

Canonical Allele Identifier: PA129398

Gene: SUMF1 HGNC NCBI

ClinVar Allele:

39646

ClinVar RCV:

RCV000023667

ClinVar Variation:

30689

HGVS (amino-acid)	Matching Registered Transcripts
NP_877437.2:p.Gly263Val	CA129397 NM_182760.4:c.788G>T