Allele Registry

Canonical Allele Identifier: PA2826687844

Gene: GUSB HGNC NCBI

ClinVar RCV:

RCV000000955

RCV003328549

RCV003398406

ClinVar Variation:

907

HGVS (amino-acid)	Matching Registered Transcripts
NP_001271219.1:p.Trp481Cys	CA339854 NM_001284290.2:c.1443G>T CA367637241 NM_001284290.2:c.1443G>C