Allele Registry

Canonical Allele Identifier: PA101740

Gene: GUSB HGNC NCBI

ClinVar Allele:

15941

ClinVar RCV:

RCV000000950

ClinVar Variation:

902

HGVS (amino-acid)	Matching Registered Transcripts
NP_000172.2:p.Arg577Leu	CA339849 NM_000181.4:c.1730G>T