Canonical Allele Identifier: PA2826687842
Gene: GUSB HGNC NCBI

Linked Data

ClinVar Variation Id: 2104924
ClinVar RCV Id: RCV003031632
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001271219.1:p.Tyr480Cys
CA367637259
NM_001284290.2:c.1439A>G