Canonical Allele Identifier: PA101147
Gene: CSTB HGNC NCBI

Linked Data

ClinVar Variation Id: 8397
ClinVar RCV Id: RCV000008905
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Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000091.1:p.Gly4Arg
CA340776
NM_000100.4:c.10G>C
CA410408703
NM_000100.4:c.10G>A