Canonical Allele Identifier: PA2573194866
Gene: GUSB HGNC NCBI

Linked Data

ClinVar Variation Id: 1369247
ClinVar RCV Id: RCV001874614

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001271219.1:p.Pro67Leu
CA159911062
NM_001284290.2:c.200C>T