Allele Registry

Canonical Allele Identifier: PA645417341

Gene: GUSB HGNC NCBI

ClinVar RCV:

RCV000360113

ClinVar Variation:

360552

HGVS (amino-acid)	Matching Registered Transcripts
NP_000172.2:p.Ala330Ser	CA4276429 NM_000181.4:c.988G>T