Canonical Allele Identifier: PA2826687858
Gene: GUSB HGNC NCBI

Linked Data

ClinVar Variation Id: 660494
ClinVar RCV Id: RCV000817695

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001271219.1:p.Ser502Arg
CA4276137
NM_001284290.2:c.1504A>C
CA367636959
NM_001284290.2:c.1506C>G
CA367636961
NM_001284290.2:c.1506C>A