Allele Registry

Canonical Allele Identifier: PA916014184

Gene: GUSB HGNC NCBI

ClinVar RCV:

RCV000293404

ClinVar Variation:

360557

HGVS (amino-acid)	Matching Registered Transcripts
NP_001271219.1:p.Ser5Pro	CA4276760 NM_001284290.2:c.13T>C