Canonical Allele Identifier: PA2826822627
Gene: GUSB HGNC NCBI

Linked Data

ClinVar Variation Id: 2432339
ClinVar RCV Id: RCV003135499

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280034.1:p.Lys409Thr
CA367637231
NM_001293105.2:c.1226A>C