Allele Registry

Canonical Allele Identifier: PA2826822511

Gene: GUSB HGNC NCBI

ClinVar RCV:

RCV001782240

RCV003388046

ClinVar Variation:

1324520

HGVS (amino-acid)	Matching Registered Transcripts
NP_001280034.1:p.Pro189Ser	CA4276354 NM_001293105.2:c.565C>T