Allele Registry

Canonical Allele Identifier: PA2826822239

Gene: GUSB HGNC NCBI

ClinVar Allele:

15935

ClinVar RCV:

RCV000000944

ClinVar Variation:

896

HGVS (amino-acid)	Matching Registered Transcripts
NP_001280033.1:p.Ala164Val	CA339840 NM_001293104.2:c.491C>T