Canonical Allele Identifier: PA2826822404
Gene: GUSB HGNC NCBI

Linked Data

ClinVar Variation Id: 92588
ClinVar Variation Id: 2742036
ClinVar RCV Id: RCV003494929

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001280033.1:p.Leu459Pro
CA145853
NM_001293104.2:c.1376T>C
CA2697557267
NM_001293104.2:c.1376_1377delinsCA