Canonical Allele Identifier: PA2826822640
Gene: GUSB HGNC NCBI

Linked Data

ClinVar Variation Id: 660494
ClinVar RCV Id: RCV000817695

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280034.1:p.Ser429Arg
CA4276137
NM_001293105.2:c.1285A>C
CA367636959
NM_001293105.2:c.1287C>G
CA367636961
NM_001293105.2:c.1287C>A