Allele Registry

Canonical Allele Identifier: PA101938

Gene: GUSB HGNC NCBI

ClinVar RCV:

RCV001782240

RCV003388046

ClinVar Variation:

1324520

HGVS (amino-acid)	Matching Registered Transcripts
NP_000172.2:p.Pro408Ser	CA4276354 NM_000181.4:c.1222C>T