Canonical Allele Identifier: PA658804514
Gene: CSTB HGNC NCBI

Linked Data

ClinVar Variation Id: 431700
ClinVar RCV Id: RCV000655934
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000091.1:p.Gly4Trp
CA321727953
NM_000100.4:c.10G>T