Allele Registry

Canonical Allele Identifier: PA101780

Gene: GUSB HGNC NCBI

ClinVar RCV:

RCV000179731

RCV003129771

ClinVar Variation:

92584

HGVS (amino-acid)	Matching Registered Transcripts
NP_000172.2:p.Asp362Asn	CA220459 NM_000181.4:c.1084G>A