Canonical Allele Identifier: PA2580107470
Gene: GUSB HGNC NCBI

Linked Data

ClinVar Variation Id: 2170077
ClinVar RCV Id: RCV003085155
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000172.2:p.Ile629Thr
CA367637214
NM_000181.4:c.1886T>C