Allele Registry

Canonical Allele Identifier: PA2826822462

Gene: GUSB HGNC NCBI

ClinVar RCV:

RCV000360113

ClinVar Variation:

360552

HGVS (amino-acid)	Matching Registered Transcripts
NP_001280034.1:p.Ala111Ser	CA4276429 NM_001293105.2:c.331G>T