Canonical Allele Identifier: PA2825094597
Gene: GUSB HGNC NCBI

Linked Data

ClinVar Variation Id: 1369247
ClinVar RCV Id: RCV001874614
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000172.2:p.Pro67Leu
CA159911062
NM_000181.4:c.200C>T