Canonical Allele Identifier: PA101708
Gene: GUSB HGNC NCBI

Linked Data

ClinVar Variation Id: 894
ClinVar RCV Id: RCV000000942 RCV000170573
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000172.2:p.Arg382Cys
CA199699
NM_000181.4:c.1144C>T