Allele Registry

Canonical Allele Identifier: PA2826687693

Gene: GUSB HGNC NCBI

ClinVar Allele:

15935

ClinVar RCV:

RCV000000944

ClinVar Variation:

896

HGVS (amino-acid)	Matching Registered Transcripts
NP_001271219.1:p.Ala208Val	CA339840 NM_001284290.2:c.623C>T