Allele Registry

Canonical Allele Identifier: PA2826687730

Gene: GUSB HGNC NCBI

ClinVar RCV:

RCV001782240

RCV003388046

ClinVar Variation:

1324520

HGVS (amino-acid)	Matching Registered Transcripts
NP_001271219.1:p.Pro262Ser	CA4276354 NM_001284290.2:c.784C>T